É um tumor raríssimo, classificado como Grau I pela OMS (Organização Mundial da Saúde), o que significa que é de baixo risco. Ele é bem delimitado e de crescimento lento, surgindo da neuro-hipófise ou do infundíbulo (partes do cérebro) e é mais comum em adultos. Ele se caracteriza pela presença de células gliais (células de suporte do sistema nervoso) tumorais, que são alongadas e em forma de fuso. Essas células formam padrões em redemoinho ou agrupamentos de feixes entrelaçados. Os sinais e sintomas incluem problemas de visão, dor de cabeça, ausência de menstruação e diminuição do desejo sexual.
Introdução
O que você precisa saber de cara
É um tumor raríssimo, classificado como Grau I pela OMS (Organização Mundial da Saúde), o que significa que é de baixo risco. Ele é bem delimitado e de crescimento lento, surgindo da neuro-hipófise ou do infundíbulo (partes do cérebro) e é mais comum em adultos. Ele se caracteriza pela presença de células gliais (células de suporte do sistema nervoso) tumorais, que são alongadas e em forma de fuso. Essas células formam padrões em redemoinho ou agrupamentos de feixes entrelaçados. Os sinais e sintomas incluem problemas de visão, dor de cabeça, ausência de menstruação e diminuição do desejo sexual.
Escala de raridade
<1/50kMuito rara
1/20kRara
1/10kPouco freq.
1/5kIncomum
1/2k
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Sinais e sintomas
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Características mais comuns
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Genética e causas
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🇧🇷 Atendimento SUS — Pituicitoma
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Publicações mais relevantes
Acromegaly in an elderly male with hepatic malignancy: a case report of a diagnostic dilemma.
Acromegaly is usually caused by a growth hormone (GH)-secreting pituitary adenoma; nonpituitary causes are rare, especially in elderly patients. Paraneoplastic insulin-like growth factor-1 (IGF-1) excess from hepatic malignancy is quite uncommon, and its coexistence with a pituitary infundibular lesion presents a diagnostic challenge. A 78-year-old diabetic man presented with coarse facial features, macroglossia, and increased interdental spacing. IGF-1 was elevated (218.6 ng/mL) with normal GH, ACTH, and prolactin. The 8 AM serum cortisol was high (36.27 μg/dL), suggesting ACTH-independent hypercortisolism. MRI brain revealed an enhancing pituitary infundibular lesion (pituicytoma vs granular cell tumor). CECT A + P exhibited a large hepatic mass with pulmonary metastases, elevated tumor markers (CEA, CA 19-9, AFP), and normal adrenal glands. Findings favored paraneoplastic IGF-1 excess and hypercortisolism from hepatic malignancy, with the pituitary lesion likely incidental. The family declined further workup, and the patient was lost to follow-up. Hepatic malignancy can rarely produce IGF-1 or cortisol-like substances, leading to acromegaly-like features and hypercortisolism independent of pituitary GH or ACTH secretion. The coexistence of paraneoplastic IGF-1 excess, ACTH-independent hypercortisolism, and an incidental pituitary lesion has not been previously reported. This case highlights the need to consider nonpituitary causes of acromegaly, especially in elderly patients with atypical biochemical or imaging findings. Non-pituitary causes of acromegaly should be considered in elderly patients with atypical biochemical profiles, as hepatic malignancy can rarely produce paraneoplastic IGF-1 excess even in the presence of incidental pituitary lesions.
Posterior transpetrosal approach to a suprasellar retroinfundibular pituicytoma: A case report and comprehensive literature review.
Pituicytomas are rare benign glial neoplasms (WHO grade I) located in the sellar or suprasellar regions, arising from the neurohypophysis and infundibular area. They typically present with symptoms due to the slow growth of the tumor, including hormonal changes, visual impairment, and headaches. This case report evaluates the effectiveness of the posterior transpetrosal approach for the resection of a retroinfundibular suprasellar pituicytoma, focusing on preserving pituitary function and minimizing surgical risks. We present a 59-year-old female with a pituicytoma diagnosed by MRI and digital subtraction angiography (DSA). Preoperative embolization was performed to reduce the tumor's vascularity. The patient underwent a left posterior transpetrosal approach for tumor resection, with key surgical steps focusing on preserving the pituitary stalk, optic chiasm, and perforating vessels. The posterior transpetrosal approach provided excellent exposure, enabling near-total resection of the tumor. The patient had no new neurological deficits postoperatively, and follow-up MRI at 6 months showed no tumor recurrence. This case demonstrates the safety and efficacy of the posterior transpetrosal approach for pituicytoma resection. The approach allowed for optimal visualization and preservation of critical structures, particularly the pituitary stalk, leading to a favorable clinical outcome. Our findings, supported by a literature review, suggest that this technique is a valuable option for tumors in retroinfundibular and suprasellar locations.
Posterior pituitary tumors and other rare entities involving the pituitary gland.
Non-neuroendocrine tumors account for around 10% of all primary neoplasms of the sella. If meningiomas, craniopharyngiomas, and germ cell tumors are excluded, the remaining lesions include a broad spectrum of uncommon, benign, and aggressive, often diagnostically challenging lesions. This review aims to summarize the essential clinicopathological features of tumors of the posterior pituitary gland, infundibulum spectrum expressing thyroid transcription factor 1, and primary sellar atypical rhabdoid teratoid tumor, and provide the criteria for their diagnosis and management.
Transnasal endoscopic removal of a pituicytoma: a case report.
Pituicytoma is an exceedingly rare tumor of the pituitary gland, classified as WHO grade 1. Its presentation varies widely, often mimicking other pituitary or sellar region tumors. This report discusses a unique case of pituicytoma in a young female presenting with a combination of visual disturbances, infertility, and endocrine dysfunction, emphasizing the role of multidisciplinary management and minimally invasive surgical techniques.
Distinctive Characteristics of Rare Sellar Lesions Mimicking Pituitary Adenomas: A Collection of Unusual Neoplasms.
Background/Objectives: Pituitary tumors account for over 90% of all sellar region masses. However, a spectrum of rare neoplastic, inflammatory, infectious, and vascular lesions-benign and malignant-can arise in the intra- and parasellar compartments and clinically and radiologically mimic PitNETs. We report a cohort of 47 such rare and cystic midline intracranial lesions, emphasizing their distinctive morphological, clinical, and imaging features and the personalized treatment strategies applied. Methods: In this retrospective single-center study, we reviewed all patients treated for suspected PitNETs via transsphenoidal approach between 2015 and 2024. Of 529 surgical cases, we excluded confirmed PitNETs, meningiomas, and classical intradural craniopharyngiomas. Collected data encompassed patient demographics, tumor characteristics, presenting symptoms, extent of resection or medical therapy, endocrine outcomes, and follow-up information. Results: Among all 529 patients who underwent surgical treatment for sellar lesions from 2015 to 2024, 47 cases (8.9%) were identified as rare or cystic masses. Forty-six underwent transsphenoidal resection; one patient with hypophysitis received corticosteroid therapy alone. Presenting symptoms included headache (n = 16), dizziness (n = 5), oculomotor disturbances (n = 2), and visual impairment (n = 17). Endocrine dysfunction was found in 30 patients, 27 of whom required hydrocortisone replacement. Histopathological diagnoses were led by colloid cysts (n = 14) and Rathke's cleft cysts (n = 11). The remaining 22 cases comprised plasmacytoma, germinoma, lymphoma, pituicytoma, inverted papilloma, metastatic carcinoma, chordoma, nasopharyngeal carcinoma, chloroma, and other rare entities. Preoperative imaging diagnosis proved incorrect in 38% (18/47) of cases, with several lesions initially misidentified as PitNETs. Conclusions: Nearly 9% of presumed PitNETs were rare, often benign or inflammatory lesions requiring distinct management. Most could be safely resected and demonstrated excellent long-term outcomes. Yet, despite advanced imaging techniques, accurate preoperative differentiation remains challenging, with over one-third misdiagnosed. Clinical red flags-such as early hormone deficits, rapid progression or atypical imaging findings-should prompt early interdisciplinary evaluation and, when indicated, image-guided biopsy to avoid unnecessary surgery and ensure tailored therapy.
Publicações recentes
Acromegaly in an elderly male with hepatic malignancy: a case report of a diagnostic dilemma.
Transnasal endoscopic removal of a pituicytoma: a case report.
Distinctive Characteristics of Rare Sellar Lesions Mimicking Pituitary Adenomas: A Collection of Unusual Neoplasms.
Histopathological Types, Clinical Presentation, Imaging Studies, Treatment Strategies, and Prognosis of Posterior Pituitary Tumors: An Updated Review.
Hypopituitarism in non-neuroendocrine pituitary tumors: a systematic review.
📚 EuropePMC125 artigos no totalmostrando 134
Acromegaly in an elderly male with hepatic malignancy: a case report of a diagnostic dilemma.
Annals of medicine and surgery (2012)Transnasal endoscopic removal of a pituicytoma: a case report.
Frontiers in oncologyDistinctive Characteristics of Rare Sellar Lesions Mimicking Pituitary Adenomas: A Collection of Unusual Neoplasms.
CancersHistopathological Types, Clinical Presentation, Imaging Studies, Treatment Strategies, and Prognosis of Posterior Pituitary Tumors: An Updated Review.
Journal of clinical medicineHypopituitarism in non-neuroendocrine pituitary tumors: a systematic review.
Reviews in endocrine & metabolic disordersThree cases of pituicytoma with a review of the literature and insight into a rare variant of ependymal pituicytoma.
Clinical neuropathologyA Rare Case of Pituicytoma During Pregnancy.
JCEM case reportsPosterior transpetrosal approach to a suprasellar retroinfundibular pituicytoma: A case report and comprehensive literature review.
Brain & spineClinical, surgical, and endocrine outcome following treatment of posterior pituitary tumors: a retrospective cohort study.
PituitaryTTF1-positive posterior pituitary tumors: a single-center experience of 10 years.
EndocrineOncocytic pituicytoma in a patient with Cushing's disease: a case report and narrative literature review.
Frontiers in endocrinologyA Steerable Microcatheter Effectively Worked in Tumor Embolization.
Journal of neuroendovascular therapy[Pituicitoma in a patient with neurofibromatosis type 1].
MedicinaSustained Response to Brigatinib in an Aggressive Relapsing Atypical Pituicytoma With ELM4-ALK Fusion.
JCO precision oncologyTTF-1 immunohistochemistry in primary CNS tumors: A systematic review.
Clinical neuropathologyPituitary spindle cell oncocytoma: Two cases report and literature review.
International journal of surgery case reportsPosterior pituitary tumors and other rare entities involving the pituitary gland.
Brain pathology (Zurich, Switzerland)Intraventricular pituicytoma: illustrative case.
Journal of neurosurgery. Case lessonsPituitary Apoplexy: Description of Medical and Surgical Treatment and Clinical, Visual, and Endocrinological Outcomes During the SARS-CoV-2 Pandemic and Over Three Years.
CureusPituitary neuroendocrine tumors and granular cell pituicytomas at autopsy: Incidence, cell types, locations, and histogenesis in 150 pituitary glands.
American journal of clinical pathology[18F]FET PET/MRI: An Accurate Technique for Detection of Small Functional Pituitary Tumors.
Journal of nuclear medicine : official publication, Society of Nuclear MedicineAn institutional experience in applying quality improvement measures to pituitary surgery: clinical and resource implications.
Neurosurgical focusCollision sellar lesion: coexistence of growth hormone-secreting pituitary neuroendocrine tumor and pituicytoma.
Polish archives of internal medicineSupra-sellar granular cell tumor: Report of a case with literature review.
International journal of surgery case reportsPituicytoma: A rare tumor of the sella. A case report and review of literature for diagnosis and management.
Surgical neurology internationalSynchronous Posterior and Anterior Pituitary Tumors: A Case Report of a Hypothetic Paracrine Relationship.
Asian journal of neurosurgeryA rare case of pituicytoma-related hyperprolactinemia due to mass effect on infundibular stalk-Case report.
International journal of surgery case reportsGranular cell tumor of the neurohypophysis presenting as a third ventricle mass.
Neuropathology : official journal of the Japanese Society of NeuropathologyEpigenetic Alteration of H3K27me3 as a Possible Oncogenic Mechanism of Central Neurocytoma.
Laboratory investigation; a journal of technical methods and pathologyPrimary papillary epithelial tumor of the sella and posterior pituitary tumor show similar (epi)genetic features and constitute a single neuro-oncological entity.
Neuro-oncologySurgical approach to the treatment of pituicytoma. Report of five cases and a literature review.
World neurosurgery: XPituitary tumours: molecular and genetic aspects.
The Journal of endocrinologyCo-existence of pituicytoma and corticotroph adenoma in a patient with Cushing's disease.
PathologyPituicytoma: A case report.
Asian journal of surgeryPituicytoma: A rare case report of sellar and suprasellar tumor.
International journal of surgery case reportsPituicytoma with pleomorphism: A case report with cytological findings.
Diagnostic cytopathologyPituicytoma Associated with Suspected Cushing's Disease: Two Case Reports and a Literature Review.
Journal of clinical medicineMultiple tumorous lesions of the pituitary gland.
Hormones (Athens, Greece)The Diagnostic Impact of Epigenomics in Pituicyte-derived Tumors: Report of an Unusual Sellar Lesion with Extensive Hemorrhage and Necrotic Debris.
Endocrine pathology[Pituicytoma: a clinicopathological analysis of five cases].
Zhonghua bing li xue za zhi = Chinese journal of pathologyRecommendation to improve the WHO classification of posterior pituitary tumors as a unique entity: evidence from a large case series.
Endocrine connections[Pituicytoma: a clinicopathological analysis of twenty-one cases].
Zhonghua bing li xue za zhi = Chinese journal of pathologySurgical management of pituicytomas: a single-center case series.
Acta neurologica BelgicaOverview of the 2022 WHO Classification of Pituitary Tumors.
Endocrine pathologyHistopathology of Pituitary Lesions.
Otolaryngologic clinics of North AmericaPituicytoma in a Young Male and Review of Literature.
Neurology IndiaOutcome of endoscopic transcortical intraventricular biopsy of isolated thickened pituitary stalk lesions in children.
Journal of neurosurgery. PediatricsPituicytoma: Four cases with unusual imaging features and a literature review.
Neuro endocrinology lettersTTF1-positive Papillary Epithelial Tumor of Pituitary: An Epithelial Variant of Pituicytoma?: Retraction.
Applied immunohistochemistry & molecular morphology : AIMMA Rare Case of Pituicytoma Presenting Cystic Formation.
Brain tumor research and treatmentGenetic and epigenetic characterization of posterior pituitary tumors.
Acta neuropathologicaPrimary Tumors of the Pituitary Gland: Radiologic-Pathologic Correlation.
Radiographics : a review publication of the Radiological Society of North America, IncIncidental Intra-Infundibular Pituicytoma.
Acta endocrinologica (Bucharest, Romania : 2005)Two challenging cases of pituicytoma.
Hormones (Athens, Greece)Clinical features, radiological profiles, pathological features and surgical outcomes of pituicytomas: a report of 11 cases and a pooled analysis of individual patient data.
Military Medical ResearchSkull Base Tumors: Neuropathology and Clinical Implications.
NeurosurgeryCo-occurrence of Pituitary Neuroendocrine Tumors (PitNETs) and Tumors of the Neurohypophysis.
Endocrine pathologyTreatment and prognostic factors of pituicytoma: a single-center experience and comprehensive literature review.
PituitaryPituicytoma: Report of three cases and a systematic literature review.
Clinical neurology and neurosurgery[The 2017 WHO classification of pituitary tumors].
Der PathologePosterior pituitary tumours: patient outcomes and determinants of disease recurrence or persistence.
Endocrine connectionsNeuropathology of Pituitary Adenomas and Sellar Lesions.
NeurosurgeryGenomics and Epigenomics of Pituitary Tumors: What Do Pathologists Need to Know?
Endocrine pathologyPituicytoma: Case report of a rare suprasellar tumor.
Indian journal of pathology & microbiologyClinical-Pathological, Immunohistochemical, and Genetic Characterization of a Series of Posterior Pituitary Tumors.
Journal of neuropathology and experimental neurologyManagement of sellar and parasellar tumors becoming symptomatic during pregnancy: a practical algorithm based on multi-center experience and systematic literature review.
PituitaryInfectious Complications of Expanded Endoscopic Transsphenoidal Surgery: A Retrospective Cohort Analysis of 100 Cases.
Journal of neurological surgery. Part B, Skull baseLimited utility of 5-ALA optical fluorescence in endoscopic endonasal skull base surgery: a multicenter retrospective study.
Journal of neurosurgeryEpithelioid Pituicytoma: Expanding the Morphologic Spectrum of a Rare Neoplasm.
Journal of neuropathology and experimental neurologyPrimary Tumors of the Posterior Pituitary Gland: A Systematic Review of the Literature in Light of the New 2017 World Health Organization Classification of Pituitary Tumors.
World neurosurgeryAdenohypophyseal hyperfunction syndromes and posterior pituitary tumors: prevalence, clinical characteristics, and pathophysiological mechanisms.
EndocrinePituicytoma associated with Cushing's disease: a case report and literature review.
Journal of surgical case reportsClinical features and endoscopic findings of granular cell tumor of the sellar region: A case report and review of the literature.
Surgical neurology internationalA rare case report of pituicytoma with biphasic pattern and admixed with scattered Herring bodies.
World journal of surgical oncologyAcellular dermal matrix as an alternative to autologous fascia lata for skull base repair following extended endoscopic endonasal approaches.
Acta neurochirurgicaA recurrent case of pituicytoma 16 years later.
Annals of the Royal College of Surgeons of EnglandConcurrent Pituicytoma, Meningioma, and Cavernomas After Cranial Irradiation for Childhood Acute Lymphoblastic Leukemia.
World neurosurgeryIntraoperative cytology of pituicytomas.
Diagnostic cytopathologyPituicytoma Associated with Acromegaly and Cushing Disease.
World neurosurgeryTTF1-positive Papillary Epithelial Tumor of Pituitary: An Epithelial Variant of Pituicytoma?
Applied immunohistochemistry & molecular morphology : AIMMThe coexistence of infundibular pituicytoma and Cushing's disease due to pituitary adenoma: A case report.
Endocrine regulationsTumors of the Neurohypophysis: One Unit's Experience and Literature Review.
World neurosurgeryA rare case of pituicytoma presenting with severe Cushing disease: A case report and review of literature.
MedicineHypothalamic Endocrine Tumors: An Update.
Journal of clinical medicineSurgical resection of granular cell tumor of the sellar region: three indications.
PituitaryPanniculitis Under Successful Targeted Inhibition of the MAPK/ERK Signaling Pathway in a Patient With BRAF V600E-mutated Spindle Cell Oncocytoma of the Pituitary Gland.
Anticancer researchRare Thyroid Transcription Factor 1-Positive Tumors of the Sellar Region: Barrow Neurological Institute Retrospective Case Series.
World neurosurgeryHistologic, immunohistochemical, and molecular features of pituicytomas and atypical pituicytomas.
Acta neuropathologica communicationsPrimary tumors of the posterior pituitary: A systematic review.
Reviews in endocrine & metabolic disordersApplication of indocyanine green fluorescence endoscopic system in transsphenoidal surgery for pituitary tumors.
Acta neurochirurgicaEndoscopic Endonasal Approach Combined with a Simultaneous Transcranial Approach for Giant Pituitary Tumors.
World neurosurgeryPosterior pituitary tumours: the spectrum of a unique entity. A clinical and histological study of a large case series.
EndocrineIs spindle cell oncocytoma a true entity or a variant of pituicytoma? A case report with review of literature.
Neurology IndiaEpithelioid pituicytoma: An unusual case report.
Surgical neurology internationalCombined Endoscopic Endonasal and Video-microscopic Transcranial Approach with Preoperative Embolization for a Posterior Pituitary Tumor.
World neurosurgeryManagement of pituicytomas: a multicenter series of eight cases.
PituitaryClinical features, diagnosis and therapy of pituicytoma: an update.
Journal of endocrinological investigationAn exceptional presentation of pituicytoma apoplexy: A case report.
Oncology lettersCorrelations between clinical hormone change and pathological features of pituicytoma.
British journal of neurosurgeryNon-adenomatous pituitary tumours mimicking functioning pituitary adenomas.
British journal of neurosurgeryHistopathologic Findings in Canine Pituitary Glands.
Veterinary pathologyLow-Grade Glioma of the Neurohypophysis: Clinical Characteristics and Surgical Outcomes.
World neurosurgeryWelcoming the new WHO classification of pituitary tumors 2017: revolution in TTF-1-positive posterior pituitary tumors.
Brain tumor pathologyFreiburg Neuropathology Case Conference : Tumor Located in the Anterior Portion of the Third Ventricle.
Clinical neuroradiologySporadic Hemangioblastoma Arising from the Infundibulum.
Journal of radiology case reportsWhat's new in pituitary pathology?
HistopathologyPituicytoma with Significant Tumor Vascularity Mimicking Pituitary Macroadenoma.
Brain tumor research and treatmentFirst Depiction of Flow Voids to Differentiate Pituicytomas from Giant Adenomas.
World neurosurgeryExtent of surgical resection and tumor size predicts prognosis in granular cell tumor of the sellar region.
Acta neurochirurgica[Pituicytoma: report of a case].
Zhonghua bing li xue za zhi = Chinese journal of pathologyThe 2017 World Health Organization classification of tumors of the pituitary gland: a summary.
Acta neuropathologicaPituicytoma: Review of commonalities and distinguishing features among TTF-1 positive tumors of the central nervous system.
Annals of diagnostic pathologyOverview of the 2017 WHO Classification of Pituitary Tumors.
Endocrine pathologyRecurrent Pituicytoma with Pseudoaneurysm: Report of a Challenging Case.
World neurosurgeryPituicytoma-An outlook on possible targeted therapies.
CNS neuroscience & therapeuticsWHO 2016 classification: changes and advancements in the diagnosis of miscellaneous primary CNS tumours.
Neuropathology and applied neurobiologyPituicytoma: A report of three cases and literature review.
Oncology lettersHistological features of pituitary adenomas and sellar region masses.
Current opinion in endocrinology, diabetes, and obesityImmunoprofiling of glial tumours of the neurohypophysis suggests a common pituicytic origin of neoplastic cells.
PituitaryCoexisting pituicytoma and pituitary adenoma: a second coincidence?
Human pathologyCoexisting pituicytoma and pituitary adenoma; a second coincidence?-reply.
Human pathologyProceedings of the 2015 National Toxicology Program Satellite Symposium.
Toxicologic pathologyPituicytoma Coexisting With Corticotroph Hyperplasia: Literature Review With One Case Report.
MedicineThe clinicopathological features of pituicytoma and the differential diagnosis of sellar glioma.
Neuropathology : official journal of the Japanese Society of NeuropathologyPituicytoma and Cushing's Disease in a 7-Year-Old Girl: A Mere Coincidence?
PediatricsSynchronous pituitary adenoma and pituicytoma.
Human pathologyA spontaneously occurring malignant pituicytoma in a male sprague dawley rat.
Journal of toxicologic pathology[Pituicytoma: a study of 3 cases with literature review].
Zhonghua bing li xue za zhi = Chinese journal of pathologyProlactin-producing pituitary adenoma with atypical spindle cell morphology: a case report.
World journal of surgical oncologyThe Expanding Spectrum of Disease Treated by the Transnasal, Transsphenoidal Microscopic and Endoscopic Anterior Skull Base Approach: A Single-Center Experience 2008-2015.
World neurosurgerySuprasellar chordoid neoplasm with expression of thyroid transcription factor 1: evidence that chordoid glioma of the third ventricle and pituicytoma may form part of a spectrum of lineage-related tumors of the basal forebrain.
Human pathologyTTF-1-positive oncocytic sellar tumor with follicle formation/ependymal differentiation: non-adenomatous tumor capable of two different interpretations as a pituicytoma or a spindle cell oncocytoma.
Brain tumor pathologySecond-stage transsphenoidal approach (TSA) for highly vascular pituicytomas in children.
Child's nervous system : ChNS : official journal of the International Society for Pediatric NeurosurgeryIntrasellar pilocytic astrocytomas: clinical, imaging, pathological, and surgical findings.
Journal of clinical neuroscience : official journal of the Neurosurgical Society of AustralasiaAssociações
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Referências e fontes
Bases de dados externas citadas neste artigo
Publicações científicas
Artigos indexados no PubMed ligados a esta doença no grafo RarasNet — título, periódico e PMID direto da fonte, sem intermediação de IA.
- Acromegaly in an elderly male with hepatic malignancy: a case report of a diagnostic dilemma.
- Posterior transpetrosal approach to a suprasellar retroinfundibular pituicytoma: A case report and comprehensive literature review.
- Posterior pituitary tumors and other rare entities involving the pituitary gland.
- Transnasal endoscopic removal of a pituicytoma: a case report.
- Distinctive Characteristics of Rare Sellar Lesions Mimicking Pituitary Adenomas: A Collection of Unusual Neoplasms.
- Histopathological Types, Clinical Presentation, Imaging Studies, Treatment Strategies, and Prognosis of Posterior Pituitary Tumors: An Updated Review.
- Hypopituitarism in non-neuroendocrine pituitary tumors: a systematic review.
Bases de dados e fontes oficiais
Identificadores e referências canônicas usadas para montar este verbete.
- ORPHA:251623(Orphanet)
- MONDO:0006372(MONDO)
- GARD:20711(GARD (NIH))
- Busca completa no PubMed(PubMed)
- Q7199535(Wikidata)
Dados compilados pelo RarasNet a partir de fontes abertas (Orphanet, OMIM, MONDO, PubMed/EuropePMC, ClinicalTrials.gov, DATASUS, PCDT/MS). Este conteúdo é informativo e não substitui avaliação médica.
Conteúdo mantido por Agente Raras · Médicos e pesquisadores podem colaborar
