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The diagnosis and treatment strategy of occipital skull mass in hemophilic patients: a rare case report and literature review

BACKGROUND: Cranial hemophilic pseudotumor (cHPT) is a very rare disease, which is easy to misdiagnose. It is also difficult to manage such patients. We reported the first case of occipital cHPT. CASE PRESENTATION: Here, we presented a rare case of an occipital bone mass in a 3-year-old boy who was...

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Autores principales: Liu, Qingyuan, Wu, Jun, Li, Chunde, Wang, Shuo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7398374/
https://www.ncbi.nlm.nih.gov/pubmed/32922908
http://dx.doi.org/10.1186/s41016-019-0155-x
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author Liu, Qingyuan
Wu, Jun
Li, Chunde
Wang, Shuo
author_facet Liu, Qingyuan
Wu, Jun
Li, Chunde
Wang, Shuo
author_sort Liu, Qingyuan
collection PubMed
description BACKGROUND: Cranial hemophilic pseudotumor (cHPT) is a very rare disease, which is easy to misdiagnose. It is also difficult to manage such patients. We reported the first case of occipital cHPT. CASE PRESENTATION: Here, we presented a rare case of an occipital bone mass in a 3-year-old boy who was diagnosed with hemophilia A. The mass was misdiagnosed as an aneurysmal bone cyst by pathological examination. After resection, the patient underwent one-stage cranioplasty. However, the patient was admitted again for hematoma caused by an invasive procedure. A second surgery and one-stage cranioplasty were performed at the same time. A follow-up 3 months after discharging showed the patient was uneventful, and the titanium mesh was well fixed. CONCLUSION: The diagnosis of cHPT requires the combining of history, radiological examination, and pathological examination. Resection is the best choice for symptomatic cHPT. Replacement treatment and less invasive treatment can make perioperative management safer. One-stage cranioplasty for resection of an occipital cHPT can improve the quality of life.
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spelling pubmed-73983742020-09-10 The diagnosis and treatment strategy of occipital skull mass in hemophilic patients: a rare case report and literature review Liu, Qingyuan Wu, Jun Li, Chunde Wang, Shuo Chin Neurosurg J Case Report BACKGROUND: Cranial hemophilic pseudotumor (cHPT) is a very rare disease, which is easy to misdiagnose. It is also difficult to manage such patients. We reported the first case of occipital cHPT. CASE PRESENTATION: Here, we presented a rare case of an occipital bone mass in a 3-year-old boy who was diagnosed with hemophilia A. The mass was misdiagnosed as an aneurysmal bone cyst by pathological examination. After resection, the patient underwent one-stage cranioplasty. However, the patient was admitted again for hematoma caused by an invasive procedure. A second surgery and one-stage cranioplasty were performed at the same time. A follow-up 3 months after discharging showed the patient was uneventful, and the titanium mesh was well fixed. CONCLUSION: The diagnosis of cHPT requires the combining of history, radiological examination, and pathological examination. Resection is the best choice for symptomatic cHPT. Replacement treatment and less invasive treatment can make perioperative management safer. One-stage cranioplasty for resection of an occipital cHPT can improve the quality of life. BioMed Central 2019-04-03 /pmc/articles/PMC7398374/ /pubmed/32922908 http://dx.doi.org/10.1186/s41016-019-0155-x Text en © The Author(s) 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Case Report
Liu, Qingyuan
Wu, Jun
Li, Chunde
Wang, Shuo
The diagnosis and treatment strategy of occipital skull mass in hemophilic patients: a rare case report and literature review
title The diagnosis and treatment strategy of occipital skull mass in hemophilic patients: a rare case report and literature review
title_full The diagnosis and treatment strategy of occipital skull mass in hemophilic patients: a rare case report and literature review
title_fullStr The diagnosis and treatment strategy of occipital skull mass in hemophilic patients: a rare case report and literature review
title_full_unstemmed The diagnosis and treatment strategy of occipital skull mass in hemophilic patients: a rare case report and literature review
title_short The diagnosis and treatment strategy of occipital skull mass in hemophilic patients: a rare case report and literature review
title_sort diagnosis and treatment strategy of occipital skull mass in hemophilic patients: a rare case report and literature review
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7398374/
https://www.ncbi.nlm.nih.gov/pubmed/32922908
http://dx.doi.org/10.1186/s41016-019-0155-x
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