Ganglioneuroma

Project: Every Child for Younger Patients With Cancer

NCT02402244

RECRUTANDO

SIOPEN BIOPORTAL, An International Registry Linked to a Virtual Biobank for Patients With Peripheral Neuroblastic Tumours

NCT05192980

RECRUTANDO

Abdominal Neuroblastoma Laparoscopic Surgery Risk Factors Stratification

NCT06296732

RECRUTANDO

An Investigational Scan (68Ga-DOTATATE PET/CT) in Diagnosing Pediatric Metastatic Neuroendocrine Tumors

NCT04040088

EM ANDAMENTO

DOTATOC PET/CT for Imaging NET Patients

NCT03583528

EM ANDAMENTO

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Outros ensaios clínicos

12 ensaios clínicos encontrados, 5 ativos.

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NCT04040088 · An Investigational Scan (68Ga-DOTATATE PET/CT) in Diagnosing…Ativo

EARLY_PHASE1

NCT03583528 · DOTATOC PET/CT for Imaging NET PatientsAtivo

NCT01999270 · Evaluation of FDOPA-PET/MRI in Pediatric Patients With CNS T…Concluído

PHASE1

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Publicações mais relevantes

Timeline de publicações

644 papers (10 anos)

Mostrando amostra de 200 publicações de um total de 644

#1

[Correlation study between tumor location and pathological subtypes of neuroblastic tumors associated with opsoclonus myoclonus ataxia syndrome].

Zhonghua er ke za zhi = Chinese journal of pediatrics2026 Mar 14

Objective: To analyze the correlation between the location and pathological subtypes of of neuroblastic tumors (NBT) associated with opsoclonus myoclonus ataxia syndrome (OMAS). Methods: A case-control study. Clinical data of 34 pediatric patients diagnosed with NBT complicated by OMAS (NBT-OMAS group), who were hospitalized in the Department of Pediatrics, Peking University First Hospital from January 2007 and December 2022 were collected retrospectively. The control group consisted of 34 age and sex-matched patients with NBT only (NBT-only group) admitted during the same period. Chi-square test or Fisher exact test was used to compare the distribution of tumor locations and pathological subtypes between the two groups. Cramer's V coefficient was applied to analyze the correlation between them. The outcomes of the patients were followed up. Results: The age of patients in the NBT-OMAS group was 18 (12, 28) months, while that of the NBT-only group was 20 (13, 31) months. In the NBT-OMAS group, 28 cases (82%) had tumors located in the paraspinal sympathetic chain and 6 cases (18%) in the adrenal glands. In the NBT-only group, 6 cases (18%) had tumors located in the adrenal glands and 28 cases (82%) in the paraspinal sympathetic chain, with a statistically significant difference between the two groups (χ2=10.69, P<0.01). The distribution of pathological subtypes of tumors in the NBT-OMAS group was as follows: 20 cases (59%) of ganglioneuroblastoma (GNB), 10 cases (29%) of neuroblastoma (NB), 4 cases (12%) of ganglioneuroma (GN). In the NBT-only group, NB was predominant with 21 cases (62%), GNB in 13 cases (38%), and no GN subtype was observed. There was a statistically significant difference between the two groups (χ2=8.59, P<0.01). In the NBT-OMAS group, the pathological subtype of tumors located in the adrenal gland was mainly NB, with 5 cases (5/6). For tumors located paravertebral to the thoracic and lumbar spine, the predominant subtype was GNB, with 8 cases (8/11) and 11 cases (11/13) respectively. As for tumors paravertebral to the sacral spine, the major subtype was NB, with 3 cases (3/4). In the NBT-only group, NB was the pathological subtype in 18 cases of adrenal gland tumors (18/19). For tumors paravertebral to the cervical spine, NB and GNB each accounted for 2 cases respectively (2/4). Tumors located paravertebral to the thoracic spine and paravertebral to the lumbar spine were all GNB for 5 cases (5/5), while those paravertebral to the sacral spine were all NB for 1 case (1/1). The Cramer's V coefficients of the tumor location and pathological subtype in the two groups were 0.65 and 0.81, respectively. The follow-up ended on December 31, 2023. In the NBT-OMAS group, 1 case had tumor recurrence and 1 case died due to tumor progression; both the recurrent and fatal tumors were located in the adrenal glands with the pathological subtype of NB. In the NBT-only group, 11 cases died of tumor progression, among which 8 cases had primary tumor located in the adrenal gland and with the pathological subtype of NB. Conclusions: In children with NBT-OMAS, tumors located in the paravertebral sympathetic chains are significantly more common than those in the adrenal gland, the pathological subtype of tumors was predominantly GNB. The tumor location was correlated with its pathological subtype. 目的：分析并发眼阵挛肌阵挛共济失调综合征（OMAS）的神经母细胞肿瘤（NBT）肿瘤发生部位与病理亚型的相关性。方法：病例对照研究。收集2007年1月至2022年12月在北京大学第一医院儿科住院且明确诊断为NBT并发OMAS的34例患儿（NBT-OMAS组）临床资料，对照组为同期入院、年龄和性别都匹配的单纯NBT患儿34例（单纯NBT组），采用χ2 检验或Fisher确切概率法比较两组肿瘤发生部位、病理亚型的分布情况，通过Cramer′s V系数比较两者的相关性，随访患儿结局。结果： NBT-OMAS组患儿年龄18（12，28）月龄，单纯NBT组年龄为20（13，31）月龄。NBT-OMAS组肿瘤发生于脊柱旁交感神经链者28例（82%）、肾上腺者6例（18%）；单纯NBT组中发生于肾上腺和脊柱旁交感神经链者分别为19例（56%）和15例（44%），两组比较差异有统计学意义（χ2=10.69，P<0.01）。NBT-OMAS组肿瘤病理亚型分布为节细胞神经母细胞瘤（GNB）20例（59%），神经母细胞瘤（NB）10例（29%），节细胞神经瘤（GN）4例（12%）；单纯NBT组病理类型主要为NB 21例（62%），GNB 13例（38%），无GN亚型，两组比较差异有统计学意义（χ2=8.59，P<0.01）。NBT-OMAS组中，6例肿瘤位于肾上腺者中5例为NB；11例位于胸椎旁者中8例为GNB；13例位于腰椎旁者中11例为GNB；4例位于骶椎旁者中3例为NB。单纯NBT组中，19例肿瘤位于肾上腺中18例为NB；4例位于颈椎旁者中NB和GNB各占2例；5例位于胸椎旁和5例位于腰椎旁者均为GNB；1例位于骶椎旁者为NB。两组肿瘤所在部位与其病理亚型的Cramer′s V系数分别为0.65、0.81。随访截至2023年12月31日，NBT-OMAS组1例肿瘤复发、1例因肿瘤进展死亡，肿瘤均位于肾上腺且病理亚型为NB；单纯NBT组有11例因肿瘤进展死亡，其中8例原发肿瘤位于肾上腺且病理亚型为NB。结论： NBT-OMAS患儿肿瘤发生于脊柱旁交感神经链者明显多于肾上腺者；肿瘤病理亚型以GNB者为主；肿瘤发生部位与其病理亚型相关。.

#2

Dysplastic cerebellar gangliocytoma: a six-decade study.

Journal of neurosurgical sciences2026 Feb

Dysplastic cerebellar gangliocytoma (DCG) is a rare cerebellar tumor glioneuronal and neuronal tumor with phosphatase and tensin homolog (PTEN) identified as a key altered gene. The aim of this study is to establish DCG diagnostic and outcome trends over a six-decade and present cases from our institution. A literature review of online databases was performed using relevant terms (January 1970-October 2024). Our institution pathology database was queried for patients with DCG (2000-2024). Data was extracted and dichotomized in adult and pediatric cases. We report three new DCG cases in addition to the 170 DCG cases reported across 97 articles over seven decades, with 52% of articles published since 2010. DCG predominantly occurred in adults (>18 years, 82%), women (59%), at mean age 9.0±6.3 years and 38.1±13.7 years in pediatric and adult patients, respectively. Balance/coordination deficit, headache and visual deficit were the most common presenting symptoms. MRI "tiger-stripe" pattern was present in 67%. Surgical resection was the treatment of choice for >97% of patients. Association with Cowden Syndrome (CS) was confirmed in 67% of patients. PTEN mutations identified in 48.3% of cases, primarily affecting chromosome 10 (10q23.3). Progression-free survival was experienced by 74% of patients and reoperation for progression needed in 3.5% of cases. DCG is a rare tumor associated with PTEN mutations. MRI aids in diagnosis and surgery ensures favorable outcomes. Standardized genetic screening and targeted therapies require further study, as they hold promise for refining diagnosis and long-term management.

#3

Atypical presentations and neurosurgical Synergy in the treatment of paravertebral tumors in children: Lessons from a single institution.

Pediatrics and neonatology2026 Jan

This study aims to evaluate the surgical management and outcomes of pediatric paravertebral tumors, particularly focusing on dumbbell tumors, within a single medical center. Employing a retrospective analysis at Taichung Veterans General Hospital from January 2016 to February 2022, we included pediatric patients diagnosed with paravertebral tumors confirmed via MRI and histopathology, who underwent surgical treatment. We aimed to assess the extent of tumor resection as the primary outcome, with postoperative complications, recurrence rates, and neurological function as secondary outcomes, utilizing descriptive statistics. In the given period, four pediatric patients, two males and two females aged 53-204 months, were treated at our institute for paravertebral tumors using CT and MRI for diagnosis. The tumors were located in the posterior mediastinum (3 patients) and retroperitoneum (1 patient), with varied MRI findings. Diagnoses included Ganglioneuroma, Schwannoma, Plexiform neurofibroma, and Spindle cell sarcoma. Treatments involved minimally invasive surgeries, with three cases using intraoperative neurological monitoring. Despite a mean operative time of 376 min and a 13-day average hospital stay, one patient experienced recurrence requiring chemotherapy, another had distant metastasis, and one died at a two-year median follow-up. Our study concludes that CT and MRI are crucial for diagnosing paravertebral tumors and planning surgery, and a multidisciplinary approach is essential for optimal functional preservation in pediatric patients. These findings emphasize the necessity for ongoing research to refine treatment strategies and improve patient outcomes in this complex clinical area.

#4

A case of colon Ganglioneuroma resembling an inverted diverticulum on endoscopy.

Digestive and liver disease : official journal of the Italian Society of Gastroenterology and the Italian Association for the Study of the Liver2026 Apr

#5

Telomere maintenance mechanisms are activated in ganglioneuroblastoma and ganglioneuroma.

Oncology letters2026 May

Telomere maintenance mechanisms (TMM) have garnered attention as a mechanism associated with the treatment resistance and poor prognosis of neuroblastoma (NB). Ganglioneuroblastoma (GNB) and ganglioneuroma (GN) are histologically classified as neuroblastic tumors (NTs) along with NB; however, few reports have addressed TMM in GNB and GN. The present study analyzed 321 NTs diagnosed in Japan, including 255 NB cases, 48 GNB cases and 18 GN cases, using a quantitative PCR-based C-circle assay for alternative lengthening of telomeres (ALT) and a telomerase reverse transcriptase (TERT) mRNA expression assay. ALT was identified in 38 NB cases (38/255, 15%) and 6 GNB cases (6/48, 12.5%), but not in GN. High TERT expression was observed in 38% (64/169), 23% (7/31) and 14% (1/7) of NB, GNB and GN cases, respectively. TMM activation, defined as ALT(+) and/or high TERT expression, occurred in 12/48 GNB cases and 1/18 GN cases, particularly in the GNB-nodular type (10/21, 48%), which was similar to 39% (100/255) of NB cases. Furthermore, TMM(+) GNBs exhibited distinct features, including a high frequency of ATRX alterations and a lower frequency of TERT rearrangements. Chromosomal aberration analysis revealed frequent 7q gain, 17q gain and 11q loss in ALT(+) NTs (83%). Overall, TMM serves as a poor prognostic marker for high-risk NB and offers valuable insights for the risk classification of GNBs.

Publicações recentes

A rare case of retroperitoneal ganglioneuroma in adult: diagnostic and management challenges.

J Surg Case Rep2026 Apr

A giant cervical ganglioneuroma in a middle-aged man: a case report.

Front Oncol2026

Not all that wheezes is asthma: A pediatric posterior mediastinal ganglioneuroma mimicking recurrent asthma.

Respir Med Case Rep2026

Ganglioneuroma in a Meller's chameleon (Triocerosmelleri).

J Comp Pathol2026 Mar 25

Telomere maintenance mechanisms are activated in ganglioneuroblastoma and ganglioneuroma.

Oncol Lett2026 May

Ver todas no PubMed

📚 EuropePMC1.208 artigos no totalmostrando 200

Telomere maintenance mechanisms are activated in ganglioneuroblastoma and ganglioneuroma.

Oncology letters

Cavitary Pulmonary Blastomycosis and an Incidental Retroperitoneal Ganglioneuroma Mimicking Metastatic Disease.

Zhonghua er ke za zhi = Chinese journal of pediatrics

[Correlation study between tumor location and pathological subtypes of neuroblastic tumors associated with opsoclonus myoclonus ataxia syndrome].

Stereotactic Body Radiation Therapy in the Management of Recurrent Unresectable Retroperitoneal Ganglioneuroma.

An Unexpected Diagnosis After a Viral Infection: A Case of a Giant Mediastinal Ganglioneuroma.

Endocrinology, diabetes & metabolism case reports

Bilateral pheochromocytoma as a late presentation of neurofibromatosis type 1.

Journal of pediatric surgery

Can indocyanine green fluorescence aid operative decision making in neuroblastic tumour surgery? Early experience from a single centre.

Digestive and liver disease : official journal of the Italian Society of Gastroenterology and the Italian Association for the Study of the Liver

A case of colon Ganglioneuroma resembling an inverted diverticulum on endoscopy.

Total laparoscopic excision of pelvic retroperitoneal ganglioneuroma: a case report and review of the literature.

Acta neuropathologica communications

Mixed gangliocytoma-pituitary neuroendocrine tumour: clinical, immunohistochemical, and molecular genetic profiles in a series of four patients.

Pathology of peripheral neuroblastic tumors.

Diagnostic pathology

Adrenal schwannomas and adrenal ganglioneuromas: our experience and CT characteristic-focused systematic review.

Endocrine

Ganglioneuroma has a potential for lymph node metastasis, not impacting recurrence.

The Journal of steroid biochemistry and molecular biology

Serum steroid profiling by LC-MS/MS in distinguishing adrenocortical carcinoma from other indeterminate adrenal masses.

Journal of spine surgery (Hong Kong)

Resection of bilateral dumbbell C2 ganglioneuroma.

A case of giant retroperitoneal ganglioneuroma encasing major vascular structures.

European spine journal : official publication of the European Spine Society, the European Spinal Deformity Society, and the European Section of the Cervical Spine Research Society

Cavernous ganglioneuroma of the thoracic spine: surgical nuances and outcomes following limited anterior resection.

Cancer research communications

Copy-Number Aberrations in Circulating Tumor DNA Enable Diagnosis and Risk Stratification of Pediatric Neuroblastic Tumors.

Zhonghua bing li xue za zhi = Chinese journal of pathology

[Clinicopathological and molecular genetic features of pediatric malignant peripheral nerve sheath tumors originating from ganglioneuroma/ganglioneuroblastoma].

Endocrine practice : official journal of the American College of Endocrinology and the American Association of Clinical Endocrinologists

Multiple Endocrine Neoplasia Type 5 due to Germline MAX Mutations: A Systematic Review of Tumor Spectrum and Clinical Features.

Mixed gangliocytoma-silent somatotroph pituitary adenoma: a rare variant with pregnancy-associated growth.

BMJ case reports

Non-Syndromic Ganglioneuromatosis of the Gallbladder, an Extremely Rare Condition: Case Report and Literature Review.

Reports (MDPI)

Endocrinology, diabetes & metabolism case reports

A potentially dangerous case of mistaken identity: giant asymptomatic composite phaeochromocytoma.

Annals of nuclear medicine

18F-FDG PET/CT manifestations of extra-adrenal retroperitoneal ganglioneuroma: a retrospective study of 21 cases.

Annals of medicine and surgery (2012)

Surgical management of a giant retrorectal ganglioneuroma via an open anterior approach: a case report.

Retroperitoneal and pelvic schwannoma/neurofibroma resection: surgical strategies and outcomes in a neurosurgical cohort.

Acta neurochirurgica

Adult retroperitoneal Ganglioneuroma: Case report of an incidental mass treated with robotic excision.

Urology case reports

Preoperative differentiation of retroperitoneal ganglioneuroma and schwannoma using an ultrasonography-based multivariable model and simplified score: development and single-center internal validation.

Acta gastroenterologica Latinoamericana

[Ganglioneuroma of the Small Intestine Mimicking Crohn's Disease].

Dumbbell ganglioneuroma of the lumbar spine: a case report and literature review.

Journal of clinical ultrasound : JCU

Atypical Polypoid Ganglioneuroma Initially Detected by Ultrasonography With Signs of Intussusception: A Case Report.

Clinical features and oncologic outcomes of primary retroperitoneal ganglioneuroma: a retrospective cohort study of 51 patients from a high-volume sarcoma center.

Histologic Response to Induction Chemotherapy in High-Risk Neuroblastoma.

Cancer medicine

Indian journal of surgical oncology

The Advancing Frontier: Robotic-Assisted Laparoscopy in Pediatric Tumor Management.

Diagnostics (Basel, Switzerland)

Colonic Ganglioneuroma-A Rare Finding During Colonoscopy.

Journal of clinical medicine

Multivisceral Resection for Suspected Adrenocortical Carcinoma.

Journal of neurosurgical sciences

Dysplastic cerebellar gangliocytoma: a six-decade study.

[Adrenal ganglioneuroma].

Arkhiv patologii

European spine journal : official publication of the European Spine Society, the European Spinal Deformity Society, and the European Section of the Cervical Spine Research Society

Giant retroperitoneal ganglioneuroma with lumbar nerve root involvement in a child: a case report and a systematic review of literature.

Laparoscopic management of multiple retroperitoneal ganglioneuromas with 5-year follow-up: a case report.

BMC urology

End-to-end deep learning model for the diagnosis and segmentation of primary retroperitoneal neoplasm: a multicenter cohort study.

EClinicalMedicine

New heights in CT differentiation of adrenal lesions and a rational definition of non-enhancement.

BMC medical imaging

3D Model-Guided Robot-Assisted Giant Presacral Ganglioneuroma Exeresis by a Uro-Neurosurgeons Team: A Case Report.

Reports (MDPI)

Open medicine (Warsaw, Poland)

Lateral transperitoneal laparoscopic adrenalectomy: A single-centre experience of 21 procedures.

Multimedia manual of cardiothoracic surgery : MMCTS

Left robotic assisted thoracic surgery (RATS) stellate ganglion ganglioneuroma resection with post-operative Harlequin syndrome.

World journal of gastrointestinal surgery

Resection of a ganglioneuroma encasing major blood vessels using three-dimensional laparoscopy combined with organ suspension: A case report.

Neuro endocrinology letters

A Rare Case: Composite Paraganglioma-Ganglioneuroma in a Neurofibromatosis 1 Patient and Literature Review.

Parapharyngeal Space Ganglioneuroma in a Child: A Report of a Rare Case.

Clinical features and surgical treatment of mediastinal masses in children: a retrospective study of 51 cases.

Frontiers in pediatrics

Complete resection of an incidentally discovered posterior mediastinal ganglioneuroma in an asymptomatic child: a case report.

Journal of clinical ultrasound : JCU

Unveiling Adrenal Ganglioneuroma in a 6-Year-Old Boy: Imaging Insights and Minimally Invasive Treatment.

Surprise Diagnosis of a Lumbar Mass: Cytological Diagnosis of Retroperitoneal Ganglioneuroma in a Rare Presentation.

Diagnostic cytopathology

Rare Presentation of Cervical Ganglioneuroma: A Case Report.

Subcostal approach using the single-port robotic system for a giant ganglioneuroma in a child.

JTCVS techniques

Adrenal ganglioneuroma: two case reports and literature review.

Clinical neurology and neurosurgery

Comparative analysis of growth hormone-secreting mixed gangliocytomas and pure growth hormone pituitary adenomas.

Composite gangliocytoma/neuroma and neuroendocrine tumour: a contemporary analysis of 71 cases shows risk factors for metastasis.

Histopathology

Predictive model based on blood cell analysis and coagulation function indicators for neuroblastic tumors staging diagnosis.

Orphanet journal of rare diseases

Genetic evaluation of five patients with ROHHAD-NET using whole genome sequencing and optical genome mapping.

Adrenal Incidentaloma Masquerading as Malignancy: A Rare Case of Ganglioneuroma with Nodal Metastasis.

Case reports in oncology

Dysplastic gangliocytoma of the cerebellum with an unusual radiological finding.

Ceskoslovenska patologie

Ganglioneuroma: a rare disease that simulates malignancy.

Medicina clinica

Case Report: Malignant transformation of ganglioneuroma in the rectovaginal septum to malignant peripheral nerve sheath tumor based on neurofibromas.

A rare presentation of a sacral mass: Ganglioneuroma.

Pediatrics and neonatology

Atypical presentations and neurosurgical Synergy in the treatment of paravertebral tumors in children: Lessons from a single institution.

Hormones (Athens, Greece)

The clinical spectrum of adrenal ganglioneuromas extends from severe hypertension to an asymptomatic incidentaloma; two cases and mini review of literature.

Surgical pathology clinics

Diagnostic Challenges and Updates in Peripheral Neuroblastic Tumors.

Journal of Indian Association of Pediatric Surgeons

Transperitoneal Laparoscopic Adrenalectomy in Children - Initial Experience in an Emerging Tertiary Center in Eastern India.

Adrenal Ganglioneuroma Masquerading as a Suspicious Adrenal Incidentaloma: A Case Report and Review of the Literature.

Virchows Archiv : an international journal of pathology

SS18::POU5F1-fused sarcoma of the parotid with divergent ganglioneuromatous differentiation-a novel manifestation of a rare tumor.

World journal of clinical cases

Precision en-bloc retroperitoneal paraganglioma resection performed laparoscopically: A case report.

Tertiary Lymphoid Structures Are Associated with Progression-Free Survival of Peripheral Neuroblastic Tumor Patients.

Cancers

The Urologic clinics of North America

Rare Adrenal Tumors and Adrenal Metastasis.

An Exophytic Pancreatic Mass Diagnosed as Ganglioneuroma.

ACG case reports journal

A rare case of a composite phaeochromocytoma-ganglioneuroma in Australia.

Synchronous Ipsilateral Adrenal and Retroperitoneal Ganglioneuroma: A Unique Case of Large Tumor Mass.

Case reports in medicine

Journal of neurosurgery. Case lessons

Stereotactic radiosurgery for brain metastases secondary to adrenal ganglioneuroblastoma: illustrative case.

Archives of pathology & laboratory medicine

Neural or Neural-Related Colorectal Lesion Incidence Varies by Site, and Multifocal Cases Are Often Syndromic: Insights From a Series of 593 Patients.

Journal of the Endocrine Society

Composite Pheochromocytoma-Paraganglioma With Ganglioneuroma: A Dual-Center Clinical Experience.

Indian journal of otolaryngology and head and neck surgery : official publication of the Association of Otolaryngologists of India

Composite Ganglioneuroma and Schwannoma of the Cervical Sympathetic Chain: A Case Report.

Hinyokika kiyo. Acta urologica Japonica

[Retroperitoneal Ganglioneuroma with Multifocal Bone Involvement in a Middle-Aged Woman].

Journal of translational medicine

Proteomic analysis reveals chromatin remodeling as a potential therapeutical target in neuroblastoma.

Retroperitoneal ganglioneuroma simulating lymphoma: An unusual case presentation.

Adrenocorticotropin-Secreting Pure Adrenal Ganglioneuroma Leading to Cushing Syndrome.

JCEM case reports

Zhurnal voprosy neirokhirurgii imeni N. N. Burdenko

Laparoscopic resection of neurogenic presacral tumors.

AACE clinical case reports

Two Cases of Composite Pheochromocytoma-Ganglioneuromas With Plasma Metanephrine Levels in the Subclinical Range Pheochromocytoma-Ganglioneuroma.

A rare case of lipomatous ganglioneuroma of the adrenal gland.

Urology case reports

The Journal of surgical research

A Single-Institution Analysis of Surveillance Practice for Low-Risk Neuroblastic Tumors.

Mature Adrenal Ganglioneuroma With Lipomatous Content: A Radiological and Histopathological Diagnostic Challenge.

Japanese journal of radiology

Advances in multimodal imaging for adrenal gland disorders: integrating CT, MRI, and nuclear medicine.

Nagoya journal of medical science

Adolescent thoracic scoliosis due to giant ganglioneuroma: a two-case report and literature review.

Andes pediatrica : revista Chilena de pediatria

[Adrenal tumors in pediatric patients treated with minimally invasive surgery].

Ampullary composite gangliocytoma/neuroma and neuroendocrine tumor management.

Endocrine-related cancer

Indian journal of pediatrics

ROHHAD NET in Retrospect: Key Lessons Learned from Five Cases.

European journal of pediatric surgery reports

Arterio-Ureteral Fistula as a Long-term Complication Following Retroperitoneal Presacral Ganglioneuroma Resection: Case Report in an Adolescent and Review of the Literature.

Journal of medical case reports

An intracranial odyssey: pediatric ganglioneuroma arising from the trigeminal ganglion: a case report and review of the literature.

Ganglioneuroma: a rare appendiceal tumour - case report and literature review.

Polish archives of internal medicine

Asymptomatic retroperitoneal ganglioneuroma adjacent to the abdominal organs and large abdominal vessels.

Dysplastic ganglion cell tumor of the right cerebellum: A case report and literature review.

Medicine

International journal of surgical pathology

Combined Ganglioneuroma-Schwannoma of the Retroperitoneum: An Exceedingly Rare Hybrid Nerve Sheath-Ganglioneural Tumor.

Toe Walking Secondary to Tethered Spinal Cord Caused by Ganglioneuroma: A Case Report.

Journal of clinical medicine

Characterisation of Paediatric Neuroblastic Tumours by Quantitative Structural and Diffusion-Weighted MRI.

Management of Ganglioneuroma and Ganglioneuroblastoma Intermixed: A United Kingdom Children's Cancer and Leukaemia Group (UK CCLG) Nationwide Study Report.

Pediatric blood & cancer

Pathologists' integration of prior biopsies of women with germline PTEN mutations may expedite the identification of this rare cancer predisposition syndrome.

Pathology

Indian journal of otolaryngology and head and neck surgery : official publication of the Association of Otolaryngologists of India

Cervical Ganglio-neuroma, a Rare Neck Mass in Pediatric Age: A Case Report.

Mixed Gangliocytoma-Pituitary Adenoma: A Systematic Review of Diagnostic Features, Clinical Management, and Surgical Outcomes.

World neurosurgery

Giant ganglioneuroma of the mediastinum: a case report.

Ganglioneuroma in Head and Neck: A Case Report of a Laryngeal Ganglioneuroma and a Systematic Review of the Literature.

Cancers

Unraveling the glycosphingolipid metabolism by leveraging transcriptome-weighted network analysis on neuroblastic tumors.

Cancer & metabolism

The American journal of gastroenterology

Solitary Colonic Ganglioneuroma With Central Depression: A Rare Case With Unique Morphology.

Adrenal Ganglioneuroma With Radiology-Pathology Correlation.

Journal of cancer research and therapeutics

Adrenal ganglioneuroma with retroperitoneal lymph node metastasis: A rare scenario.

Ganglioneuroma of the cervical sympathetic chain: A case report and review of literature.

An extremely rare case of presacral ganglioneuroma in a young male with lower back pain: First case report from Iraq.

Case Report: Adrenal schwannoma associated with ganglioneuroma.

Vasoactive Intestinal Peptide-Producing Neuroblastic Tumors: A Rare Cause of Refractory Diarrhea.

International journal of ophthalmology

Bilateral choroidal ganglioneuroma: a comprehensive analysis of vision decline in a 6-year-old boy.

Adrenal ganglioneuroma with nodal metastases on 123I-MIBG SPECT/CT and 18F-FDG PET/CT.

Invasive trigeminal ganglioneuroma: A case report and review of the literature.

Acta radiologica open

Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery

Spinal ganglioneuroma: a rare and challenging tumor in the pediatric population.

Laparoscopic resection for retroperitoneum ganglioneuroma with Supine hypotension syndrome.

Surgical case reports

Paravertebral Ganglioneuroma in Pediatric Age: A Case Report.

Case report: Treatment response of NF-1-associated bladder ganglioneuroma to trametinib.

Giant mediastinal ganglioneuroma in adolescents.

Two rare cases of giant ganglioneuroma of the posterior mediastinum in overweight children.

Esophageal ganglioneuromatosis; a rare cause of intractable esophageal stenosis: a case report.

BMC pediatrics

Annals of agricultural and environmental medicine : AAEM

Ganglioneuromatous polyposis associated with type 2 B multiple endocrine neoplasia (MEN 2B) - case report.

Pediatrics international : official journal of the Japan Pediatric Society

Successful endoscopic approach for peripheral neuroblastic tumors in children.

Journal of neuropathology and experimental neurology

Mixed pituitary adenoma/pituitary neuroendocrine tumor-gangliocytoma: Immunohistochemical insights.

Indian journal of pathology & microbiology

Expression of GD2 and GD3 in peripheral neuroblastic tumors.

Abdominal radiology (New York)

A head-to-head comparison of computed tomography- and magnetic resonance imaging-based radiomics in assessing pediatric peripheral neuroblastic tumor cell behavior.

Giant Ganglioneuroma of the Lumbar Spine: A Rare Cause of Radiculopathy.

Case reports in surgery

Journal of back and musculoskeletal rehabilitation

Cervical ganglioneuroma as a rare cause of cervicogenic headache: A case report and literature review.

Rare adrenal incidentaloma: ganglioneuroma.

Robotic thoracic surgery for neurogenic tumors.

Journal of neurosurgery

SAGE open medical case reports

Large retroperitoneal ganglioneuroma revealed by a left ovarian endometrioma: A case report.

Spinal ganglioneuroma with extension to the brachial plexus. The challenges for total surgical excision, a case report.

Clinical journal of gastroenterology

Multiple endocrine neoplasia type 2B diagnosed after small intestinal volvulus with progressive megacolon in an adolescent.

Massive Silent abdominal ganglioneuroma in the setting of non-Hodgkin lymphoma : A rare case report.

A novel method of tunneling retroperitoneoscopic adrenalectomy: a prospective study.

BMC urology

Zhonghua bing li xue za zhi = Chinese journal of pathology

[Intraspinal composite gangliocytoma/neuroma and neuroendocrine tumor with vascular malformation: report of a case].

Neurosurgical focus: Video

Combined unilateral biportal endoscopy and video-assisted thoracoscopic surgery for complete excision of a T3-T4 right ganglioneuroma.

Ultrasound in medicine & biology

A Preliminary Study on the Application of Contrast-Enhanced Ultrasonography in Children With Peripheral Neuroblastic Tumors.

Indian journal of otolaryngology and head and neck surgery : official publication of the Association of Otolaryngologists of India

Solitary Ganglioneuromatous Hamartoma Tongue in a Newborn - A Rare Entity.

Laryngeal Ganglioneuromatosis in a Child With Multiple Endocrine Neoplasia Type 2B (MEN2B): Case Report and Review of Literature.

AACE clinical case reports

A Woman with Bilateral Pheochromocytoma and Tuberous Sclerosis Complex.

Neuroganglioma in the posterior mediastinum: an incidental discovery.

Clinical features and treatment options for pediatric adrenal incidentalomas: a retrospective single center study.

BMC pediatrics

Revista espanola de enfermedades digestivas

Double-balloon enteroscopy for the detection of GIST in a patient with type 1 neurofibromatosis.

Kyobu geka. The Japanese journal of thoracic surgery

[Surgically Resected Cases of Mediastinal Ganglioneuroma Detected in Adults].

The Journal of craniofacial surgery

Cervical Ganglioneuroma Associated With Neurofibromatosis Type 1.

Robotic excision of a retrocaval ancient schwannoma: a case report.

Indian journal of otolaryngology and head and neck surgery : official publication of the Association of Otolaryngologists of India

Ganglioneuroma of the Cervical Sympathetic Chain - A Rare Occurrence.

Benign paraspinal ganglioneuroma with paraneoplastic opsoclonus myoclonus syndrome.

BMJ case reports

A case of thoracic intraspinal ganglioneuroma with intermittent fever as the main symptom.

Retroperitoneal Peripancreatic Ganglioneuroma Encasing the Celiac Trunk and Superior Mesenteric Artery.

Appendiceal ganglioneuroma incidentally found during resection of recurrent rectal cancer: case report and review of the literature.

[Intestinal ganglioneuromatosis as an early extra-endocrine manifestation of type 2B multiple endocrine neoplasia].

Problemy endokrinologii

Anti-metabolic glutamate receptor 5 encephalitis with gangliocytoma: a case and review of the literature.

BMC neurology

Journal of robotic surgery

Robotic-assisted surgery for gynecological indications in children and adolescents: European multicenter report.

A case report of multimodal ultrasound imaging in the diagnosis of giant retroperitoneal ganglioneuroma.

Cancer innovation

Indian journal of urology : IJU : journal of the Urological Society of India

Synchronous ipsilateral adrenal cortical adenoma and ganglioneuroma: A case report.

Acta bio-medica : Atenei Parmensis

Diagnostic imaging of a rare case of incidental adrenal ganglioneuroma.

Ganglioneuroma presents as the absence of sweating on the face and the opposite trunk in a child.

Pediatric pulmonology

N6-methyladenosine-mediated overexpression of long noncoding RNA ADAMTS9-AS2 triggers neuroblastoma differentiation via regulating LIN28B/let-7/MYCN signaling.

JCI insight

Internal medicine (Tokyo, Japan)

Colorectal Ganglioneuromas Associated with Cowden Syndrome.

Journal of cancer research and clinical oncology

Epidemiological and clinical characteristics of children with peripheral neuroblastic tumors: a study on a Moroccan population.

Composite paraganglioma-ganglioneuroma with atypical catecholamine profile and phenylethanolamine N-methyltransferase expression: a case report and literature review.

Endocrine journal

Current pediatric reviews

Late Relapse in Neuroblastoma: Case Report and Review of the Literature.

A not so incidental 'incidentaloma' - pediatric ganglioneuroma-associated cerebellar degeneration and super-refractory status epilepticus: case report and literature review.

Frontiers in neurology

Localized Multifocal Retroperitoneal Ganglioneuroma with an Infiltrative Appearance on Imaging: A Case Report.

Case reports in oncology

A rare entity: Ganglioneuroma of the prostate.

Urology case reports

Journal of laparoendoscopic & advanced surgical techniques. Part A

Laparoscopic Transperitoneal Adrenalectomy for Adrenal Tumors in Children: Technical Considerations and Surgical Experience.

Journal of pediatric surgery

Ganglioneuromas in Childhood: Hacettepe Experience With 70 Cases.

Medical oncology (Northwood, London, England)

Musashi-2 (MSI2) promotes neuroblastoma tumorigenesis through targeting MYC-mediated glucose-6-phosphate dehydrogenase (G6PD) transcriptional activation.

Preoperative differentiation of mediastinum and retroperitoneum ganglioneuroma from schwannoma with clinical data and enhanced CT: developing a multivariable prediction model.

Clinical radiology

Laparoscopic resection of ganglioneuroma from the hepatoduodenal ligament: A case report.

Pathologie (Heidelberg, Germany)

[Peripheral neuroblastic tumors in childhood].

A Sizeable Adrenal Ganglioneuroma: A Case Report.

A case report on POEMS syndrome with high parathyroid hormone and repeated surgery, a rare presentation of a rare disease.

Single-cell transcriptome sequencing reveals tumor heterogeneity in family neuroblastoma.

Frontiers in immunology

Computer-assisted resection of multifocal primary neuroblastic tumors: A case report.

Journal of clinical medicine

Nonspecific Gastrointestinal Symptoms as the First Sign of Ganglioneuroblastoma Intermixed-Case Report and Literature Review.

Operative challenges in a gigantic ganglioneuroma of the posterior mediastinum with mediastinal compression.

Overreliance on Radiological Findings Leading to Misdiagnosed Giant Retroperitoneal Ganglioneuroma: A Case Report and Literature Review.

Retroperitoneal ganglioneuroma: A five-case series from a single Tunisian center.

Revista espanola de enfermedades digestivas

Coexistence of a small bowel gastrointestinal stromal tumor, small bowel adenocarcinoma and ganglioneuroma in a patient with neurofibromatosis type I caused intussusception.

Journal of neuropathology and experimental neurology

Maturation of metastases in peripheral neuroblastic tumors (neuroblastoma) of children.

Composite pheochromocytoma associated with neurofibromatosis type 1.

IJU case reports

International journal of endocrinology and metabolism

Neck Ganglioneuroma Mimicking a Thyroid Nodule in a Four-Year-Old Child: A Case Report and Review of the Literature.

World journal for pediatric & congenital heart surgery

En Bloc Resection of a Giant Ganglioneuroma of the Chest Through Clamshell Thoracotomy.

Spinal Ganglioneuroma: A Systematic Review of the Literature.

World neurosurgery

Neuropathology : official journal of the Japanese Society of Neuropathology

Neuropil-like islands are a possible pathogenetic link between glioblastoma and gangliocytoma/ganglioglioma in a case of synchronous bilateral brain tumors.

Indian journal of otolaryngology and head and neck surgery : official publication of the Association of Otolaryngologists of India

Intraparotid Ganglioneuroma: A rare case report.

Indian journal of thoracic and cardiovascular surgery

Ganglioneuroma presenting as subpulmonic effusion-a differential to consider?

Image-defined risk factors in localized thoracic neuroblastoma and ganglioneuroma.

Pediatric blood & cancer

Adrenal ganglioneuroma: Features and outcomes of cases series.

Diagnostics (Basel, Switzerland)

Imaging of Ganglioneuroma: A Literature Review and a Rare Case of Cystic Presentation in an Adolescent Girl.

Diagnosis of PTEN mosaicism: the relevance of additional tumor DNA sequencing. A case report and review of the literature.

BMC medical genomics

Experimental and clinical endocrinology & diabetes : official journal, German Society of Endocrinology [and] German Diabetes Association

Clinical Characteristics and Long-Term Outcomes of Adrenal Tumors in Children and Adolescents.

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