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Systemic sclerosis associated with colliquative necrosis in the cerebellum
BACKGROUND: The scleroderma is a complex autoimmune collagen disorder that can affect many organs simultaneously, as it occurs in the systemic sclerosis (SS), or only the skin, as it occurs in the localized scleroderma (LS). The neurological presentation is extremely uncommon, and even more uncommon...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Medknow Publications & Media Pvt Ltd
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5402329/ https://www.ncbi.nlm.nih.gov/pubmed/28480106 http://dx.doi.org/10.4103/sni.sni_401_16 |
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author | Ricci, Alessandro Di Vitantonio, Hambra De Paulis, Danilo Del Maestro, Mattia Dehcordi, Soheila Raysi Murrone, Domenico Coletti, Gino Calvisi, Giuseppe Galzio, Renato Juan |
author_facet | Ricci, Alessandro Di Vitantonio, Hambra De Paulis, Danilo Del Maestro, Mattia Dehcordi, Soheila Raysi Murrone, Domenico Coletti, Gino Calvisi, Giuseppe Galzio, Renato Juan |
author_sort | Ricci, Alessandro |
collection | PubMed |
description | BACKGROUND: The scleroderma is a complex autoimmune collagen disorder that can affect many organs simultaneously, as it occurs in the systemic sclerosis (SS), or only the skin, as it occurs in the localized scleroderma (LS). The neurological presentation is extremely uncommon, and even more uncommon are the symptoms of the scleroderma in the cerebellum. CASE DESCRIPTION: We report the case of a 56-year-old male with cerebellar lesions mimicking a brain abscess. After surgical excision, the histopathological diagnosis deposed for an ischemic necrosis caused by a vasculopathy. All the bacteriological and viral exams were negative, whereas the rheumatologic tests were compatible with the scleroderma pattern. CONCLUSION: Up to now, the literature has described only 5 cases of scleroderma in the posterior cranial fossa. The authors report a case of SS causing colliquative necrosis in the cerebellum. Pathogenetic mechanisms, clinical aspects, and radiological features are discussed along with the pertinent literature. |
format | Online Article Text |
id | pubmed-5402329 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Medknow Publications & Media Pvt Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-54023292017-05-05 Systemic sclerosis associated with colliquative necrosis in the cerebellum Ricci, Alessandro Di Vitantonio, Hambra De Paulis, Danilo Del Maestro, Mattia Dehcordi, Soheila Raysi Murrone, Domenico Coletti, Gino Calvisi, Giuseppe Galzio, Renato Juan Surg Neurol Int Unique Case Observations: Case Report BACKGROUND: The scleroderma is a complex autoimmune collagen disorder that can affect many organs simultaneously, as it occurs in the systemic sclerosis (SS), or only the skin, as it occurs in the localized scleroderma (LS). The neurological presentation is extremely uncommon, and even more uncommon are the symptoms of the scleroderma in the cerebellum. CASE DESCRIPTION: We report the case of a 56-year-old male with cerebellar lesions mimicking a brain abscess. After surgical excision, the histopathological diagnosis deposed for an ischemic necrosis caused by a vasculopathy. All the bacteriological and viral exams were negative, whereas the rheumatologic tests were compatible with the scleroderma pattern. CONCLUSION: Up to now, the literature has described only 5 cases of scleroderma in the posterior cranial fossa. The authors report a case of SS causing colliquative necrosis in the cerebellum. Pathogenetic mechanisms, clinical aspects, and radiological features are discussed along with the pertinent literature. Medknow Publications & Media Pvt Ltd 2017-04-05 /pmc/articles/PMC5402329/ /pubmed/28480106 http://dx.doi.org/10.4103/sni.sni_401_16 Text en Copyright: © 2017 Surgical Neurology International http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 3.0 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 | Unique Case Observations: Case Report Ricci, Alessandro Di Vitantonio, Hambra De Paulis, Danilo Del Maestro, Mattia Dehcordi, Soheila Raysi Murrone, Domenico Coletti, Gino Calvisi, Giuseppe Galzio, Renato Juan Systemic sclerosis associated with colliquative necrosis in the cerebellum |
title | Systemic sclerosis associated with colliquative necrosis in the cerebellum |
title_full | Systemic sclerosis associated with colliquative necrosis in the cerebellum |
title_fullStr | Systemic sclerosis associated with colliquative necrosis in the cerebellum |
title_full_unstemmed | Systemic sclerosis associated with colliquative necrosis in the cerebellum |
title_short | Systemic sclerosis associated with colliquative necrosis in the cerebellum |
title_sort | systemic sclerosis associated with colliquative necrosis in the cerebellum |
topic | Unique Case Observations: Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5402329/ https://www.ncbi.nlm.nih.gov/pubmed/28480106 http://dx.doi.org/10.4103/sni.sni_401_16 |
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