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Castleman's disease: A rare case report and review of literature

Castleman's disease – also known as giant lymph node hyperplasia – is a rare pathology, poorly understood. Described for the first time in 1954, it is considered a lymphoproliferative disorder that manifests without any other obvious symptoms and may be confused with other causes of lymph nodal...

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Autor principal: Saadallah, Mohamed Abdelraouf Hassan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9193861/
http://dx.doi.org/10.1016/j.ijscr.2022.107282
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author Saadallah, Mohamed Abdelraouf Hassan
author_facet Saadallah, Mohamed Abdelraouf Hassan
author_sort Saadallah, Mohamed Abdelraouf Hassan
collection PubMed
description Castleman's disease – also known as giant lymph node hyperplasia – is a rare pathology, poorly understood. Described for the first time in 1954, it is considered a lymphoproliferative disorder that manifests without any other obvious symptoms and may be confused with other causes of lymph nodal enlargement. We are reporting in this paper the case of a 30-year-old Maldivian female who presented to our surgical OPD with a right cervical large solitary soft tissue lesion. All the investigations were negative except for a large highly vascularized unicentric soft tissue mass measuring around 4 cm in the anterior triangle of the neck seen by the ultrasound separable from all other surroundings. An excisional biopsy & complete resection was done under general anesthesia in the operation theater of a Maldivian Regional hospital. Unicentric Castleman's disease as a diagnosis was confirmed based on the final histopathological study of the specimen, and the absence of other cervical and extra-cervical lymphadenopathy. The patient doesn't have recurrence or newly developed lymph nodes at the time of reporting this article.
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spelling pubmed-91938612022-06-15 Castleman's disease: A rare case report and review of literature Saadallah, Mohamed Abdelraouf Hassan Int J Surg Case Rep Case Report Castleman's disease – also known as giant lymph node hyperplasia – is a rare pathology, poorly understood. Described for the first time in 1954, it is considered a lymphoproliferative disorder that manifests without any other obvious symptoms and may be confused with other causes of lymph nodal enlargement. We are reporting in this paper the case of a 30-year-old Maldivian female who presented to our surgical OPD with a right cervical large solitary soft tissue lesion. All the investigations were negative except for a large highly vascularized unicentric soft tissue mass measuring around 4 cm in the anterior triangle of the neck seen by the ultrasound separable from all other surroundings. An excisional biopsy & complete resection was done under general anesthesia in the operation theater of a Maldivian Regional hospital. Unicentric Castleman's disease as a diagnosis was confirmed based on the final histopathological study of the specimen, and the absence of other cervical and extra-cervical lymphadenopathy. The patient doesn't have recurrence or newly developed lymph nodes at the time of reporting this article. Elsevier 2022-06-07 /pmc/articles/PMC9193861/ http://dx.doi.org/10.1016/j.ijscr.2022.107282 Text en © 2022 The Author https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Case Report
Saadallah, Mohamed Abdelraouf Hassan
Castleman's disease: A rare case report and review of literature
title Castleman's disease: A rare case report and review of literature
title_full Castleman's disease: A rare case report and review of literature
title_fullStr Castleman's disease: A rare case report and review of literature
title_full_unstemmed Castleman's disease: A rare case report and review of literature
title_short Castleman's disease: A rare case report and review of literature
title_sort castleman's disease: a rare case report and review of literature
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9193861/
http://dx.doi.org/10.1016/j.ijscr.2022.107282
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