Literature DB >> 22150165

Intracranial germ cell tumours. A review with special reference to endocrine manifestations.

Tina Jorsal1, Mikael Rørth.   

Abstract

EPIDEMIOLOGY: Intracranial germ cell tumours (icGCTs) represent 3-15% of primary paediatric intracranial neoplasms with a considerable geographical variation in incidence. Ninety percent of patients diagnosed with icGCTs are under 20 years of age. PATHOLOGY: Histologic characteristics and investigation of the tumour markers β-human chorionic gonadotropin (β-hCG) and alpha-fetoprotein (AFP) help define the different categories of icGCTs. The tumours are divided into two major groups called germinomas and non-germinomatous GCTs (NGGCTs). CLINICAL
PRESENTATION: The clinical symptoms depend on the size and location of tumour in the brain, which is most commonly in the pineal or suprasellar region. Pineal GCTs often present with neurological symptoms because of their tendency to cause increased intracranial pressure. Suprasellar GCTs are often accompanied by endocrine abnormalities such as diabetes insipidus (DI), growth retardation and precocious or delayed puberty. DIAGNOSIS: A combination of clinical findings, endocrine and tumour marker evaluation, spinal fluid cytology, magnetic resonance imaging (MRI) and biopsy helps verifying the diagnosis of an icGCT. A summary of published data (n = 97) revealed that >90% of patients at diagnosis had at least one endocrine abnormality, DI being the most common (>80%). TREATMENT: Classification of tumour is important for choice of treatment and for prognosis. A combination of chemotherapy and radiotherapy is often used, since most icGCTs have a great sensitivity to these treatment modalities.
CONCLUSION: Endocrine symptoms are very frequently appearing in patients with icGCTs and they can present long before neuroimaging verification of tumour is possible. It is of the outmost importance to have the diagnosis of icGCTs in mind when children, adolescents and young adults are presenting with endocrine irregularities, because most icGCTs are very sensitive to radiotherapy and chemotherapy, and early onset of treatment is important in order to minimize morbidity and mortality.

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Year:  2012        PMID: 22150165     DOI: 10.3109/0284186X.2011.586000

Source DB:  PubMed          Journal:  Acta Oncol        ISSN: 0284-186X            Impact factor:   4.089


  21 in total

Review 1.  Primary CNS germ cell tumors: current epidemiology and update on treatment.

Authors:  Jigisha P Thakkar; Lita Chew; J Lee Villano
Journal:  Med Oncol       Date:  2013-02-24       Impact factor: 3.064

2.  Growth Hormone Deficiency in Childhood Intracranial Germ Cell Tumor Survivors.

Authors:  Diana W Lone; Karim T Sadak; Bradley S Miller; Jeannette M Sample; Aubrey K Hubbard; Caryn Wolter; Michelle Roesler; Michelle Nuno; Jenny N Poynter
Journal:  J Endocrinol Metab       Date:  2022-06-27

3.  Neuroimaging diagnosis of pineal region tumors-quest for pathognomonic finding of germinoma.

Authors:  Ryuji Awa; Francia Campos; Kazunori Arita; Kazuhiko Sugiyama; Atsushi Tominaga; Kaoru Kurisu; Fumiyuki Yamasaki; Prasanna Karki; Hiroshi Tokimura; Yoshihiko Fukukura; Yukihiko Fujii; Ryosuke Hanaya; Tatsuki Oyoshi; Hirofumi Hirano
Journal:  Neuroradiology       Date:  2014-04-29       Impact factor: 2.804

4.  Primary Central Nervous System Germ Cell Tumors: A Review and Update.

Authors:  Kaleigh Fetcko; Mahua Dey
Journal:  Med Res Arch       Date:  2018-03-15

Review 5.  Primary intracranial germ-cell tumors in adults: a practical review.

Authors:  Jacoline E C Bromberg; Brigitta G Baumert; Filip de Vos; Johanna M M Gijtenbeek; Erkan Kurt; Anneke M Westermann; Pieter Wesseling
Journal:  J Neurooncol       Date:  2013-03-23       Impact factor: 4.130

Review 6.  Matrix metalloproteinases (MMPs) and their tissue inhibitors (TIMPs) in the tumors of central nervous system (CNS).

Authors:  Marta Lukaszewicz-Zając; Barbara Mroczko; Johannes Kornhuber; Piotr Lewczuk
Journal:  J Neural Transm (Vienna)       Date:  2013-12-24       Impact factor: 3.575

7.  Incidence of intracranial germ cell tumors by race in the United States, 1992-2010.

Authors:  Jenny N Poynter; Rachel Fonstad; Jakub Tolar; Logan G Spector; Julie A Ross
Journal:  J Neurooncol       Date:  2014-08-03       Impact factor: 4.130

8.  Synchronous pituitary and pineal gland lesions presenting with panhypopituitarism in a patient with widespread colorectal cancer: a case report.

Authors:  Tristan Struja; Joël Capraro
Journal:  Oxf Med Case Reports       Date:  2021-05-24

9.  Central nervous system tumors: a single center pathology review of 34,140 cases over 60 years.

Authors:  Liang Chen; Xiang Zou; Yin Wang; Ying Mao; Liangfu Zhou
Journal:  BMC Clin Pathol       Date:  2013-05-02

10.  Chorionic gonadotropin and its receptor are both expressed in human retina, possible implications in normal and pathological conditions.

Authors:  Sladjana Dukic-Stefanovic; Jan Walther; Sebastian Wosch; Gerolf Zimmermann; Peter Wiedemann; Henry Alexander; Thomas Claudepierre
Journal:  PLoS One       Date:  2012-12-19       Impact factor: 3.240

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