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Late recurrence of primary cerebellar germinoma at unusual site after complete response to radiotherapy
BACKGROUND: The primary cerebellar germinoma is exceptional and difficult to diagnose preoperatively. Its recurrence at the middle cranial fossa after complete response to radiotherapy is unique and associated with a poor prognosis. This article aims to report the successful management of the late r...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Scientific Scholar
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8645499/ https://www.ncbi.nlm.nih.gov/pubmed/34877035 http://dx.doi.org/10.25259/SNI_663_2021 |
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author | Kieu, Hung Dinh Van Dang, Duong Le, Tam Duc |
author_facet | Kieu, Hung Dinh Van Dang, Duong Le, Tam Duc |
author_sort | Kieu, Hung Dinh |
collection | PubMed |
description | BACKGROUND: The primary cerebellar germinoma is exceptional and difficult to diagnose preoperatively. Its recurrence at the middle cranial fossa after complete response to radiotherapy is unique and associated with a poor prognosis. This article aims to report the successful management of the late recurrence of primary cerebellar germinoma at an unusual site after 4 years of complete response to radiotherapy. CASE DESCRIPTION: A 22-year-old male was admitted to our hospital with complaints of severe headache and loss of balance. Brain magnetic resonance imaging (MRI) showed a triventricular hydrocephalus due to a 45x50mm cerebellar mass. Our preliminary diagnosis was medulloblastoma. First, we placed a ventriculoperitoneal shunt with the medium-pressure valve, and then we used midline suboccipital craniotomy to remove the tumor completely. The histopathology was germinoma. The patient received 24 Gy craniospinal irradiation (CSI) with a 16 Gy boost to the primary site and had an MRI follow-up every six months. After a 4-year follow-up, he complained of recurrent severe headaches. The brain MRI illustrated a 62 × 61 mm temporal mass. We extirpated this tumor, and histopathology again revealed germinoma. After that, the patient received induction radiotherapy. The 1-year postoperative MRI showed no tumor remnant. At the time of writing, the patient had no headache and no neurological deficits. CONCLUSION: Regular follow-ups with routine neuroaxis MRI should be recommended to detect recurrence early for all patients with intracranial germinomas. Surgical resection, if possible, and subsequent CSI are the most effective salvage treatment for recurrent germinoma. |
format | Online Article Text |
id | pubmed-8645499 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Scientific Scholar |
record_format | MEDLINE/PubMed |
spelling | pubmed-86454992021-12-06 Late recurrence of primary cerebellar germinoma at unusual site after complete response to radiotherapy Kieu, Hung Dinh Van Dang, Duong Le, Tam Duc Surg Neurol Int Case Report BACKGROUND: The primary cerebellar germinoma is exceptional and difficult to diagnose preoperatively. Its recurrence at the middle cranial fossa after complete response to radiotherapy is unique and associated with a poor prognosis. This article aims to report the successful management of the late recurrence of primary cerebellar germinoma at an unusual site after 4 years of complete response to radiotherapy. CASE DESCRIPTION: A 22-year-old male was admitted to our hospital with complaints of severe headache and loss of balance. Brain magnetic resonance imaging (MRI) showed a triventricular hydrocephalus due to a 45x50mm cerebellar mass. Our preliminary diagnosis was medulloblastoma. First, we placed a ventriculoperitoneal shunt with the medium-pressure valve, and then we used midline suboccipital craniotomy to remove the tumor completely. The histopathology was germinoma. The patient received 24 Gy craniospinal irradiation (CSI) with a 16 Gy boost to the primary site and had an MRI follow-up every six months. After a 4-year follow-up, he complained of recurrent severe headaches. The brain MRI illustrated a 62 × 61 mm temporal mass. We extirpated this tumor, and histopathology again revealed germinoma. After that, the patient received induction radiotherapy. The 1-year postoperative MRI showed no tumor remnant. At the time of writing, the patient had no headache and no neurological deficits. CONCLUSION: Regular follow-ups with routine neuroaxis MRI should be recommended to detect recurrence early for all patients with intracranial germinomas. Surgical resection, if possible, and subsequent CSI are the most effective salvage treatment for recurrent germinoma. Scientific Scholar 2021-11-02 /pmc/articles/PMC8645499/ /pubmed/34877035 http://dx.doi.org/10.25259/SNI_663_2021 Text en Copyright: © 2021 Surgical Neurology International https://creativecommons.org/licenses/by-nc-sa/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution-Non Commercial-Share Alike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as the author is credited and the new creations are licensed under the identical terms. |
spellingShingle | Case Report Kieu, Hung Dinh Van Dang, Duong Le, Tam Duc Late recurrence of primary cerebellar germinoma at unusual site after complete response to radiotherapy |
title | Late recurrence of primary cerebellar germinoma at unusual site after complete response to radiotherapy |
title_full | Late recurrence of primary cerebellar germinoma at unusual site after complete response to radiotherapy |
title_fullStr | Late recurrence of primary cerebellar germinoma at unusual site after complete response to radiotherapy |
title_full_unstemmed | Late recurrence of primary cerebellar germinoma at unusual site after complete response to radiotherapy |
title_short | Late recurrence of primary cerebellar germinoma at unusual site after complete response to radiotherapy |
title_sort | late recurrence of primary cerebellar germinoma at unusual site after complete response to radiotherapy |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8645499/ https://www.ncbi.nlm.nih.gov/pubmed/34877035 http://dx.doi.org/10.25259/SNI_663_2021 |
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