Literature DB >> 20588244

Germ cell tumor presenting as sellar mass with suprasellar extension and long history of hypopituitarism.

Leandro Kasuki Jomori de Pinho1, Leonardo Vieira Neto, Leila Maria Cardão Chimelli, Emerson Leandro Gasparetto, Leila Warszawski, Antônio Aversa Dutra do Souto, Mônica R Gadelha.   

Abstract

OBJECTIVE: Primary central nervous system germ cell tumors are rare neoplasms usually located in the pineal and/or suprasellar region. Pure germinomas do not usually secrete beta-human chorionic gonadotropin hormone (beta-HCG) or alpha-fetoprotein (AFP) and diagnosis is made a few weeks or months after beginning of symptoms. CASE: Here we report a case of a pure germinoma in a 20 year-old woman presenting as a sellar mass with suprasellar extension, abnormal serum beta-HCG and a long history of polyuria and polydipsia (4 years), that was initially diagnosed as a pituitary macroadenoma.
CONCLUSION: This presentation highlights the importance of thinking in alternative diagnosis to pituitary adenoma when diabetes insipidus is the initial symptom.

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Year:  2010        PMID: 20588244

Source DB:  PubMed          Journal:  Neuro Endocrinol Lett        ISSN: 0172-780X            Impact factor:   0.765


  1 in total

Review 1.  Pineal region tumors: pathophysiological mechanisms of presenting symptoms.

Authors:  Ioannis N Mavridis; Efstratios-Stylianos Pyrgelis; Eleni Agapiou; Maria Meliou
Journal:  Am J Transl Res       Date:  2021-06-15       Impact factor: 4.060

  1 in total

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