AccScience Publishing / EJMO / Volume 2 / Issue 3 / DOI: 10.14744/ejmo.2018.14632
CASE REPORT

Castleman's Disease Associated with Pemphigus Vulgaris: Remains Retrospectively Diagnosed Entity

Dhaivat K Vaishnav1
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1 Department of GI and HPB Surgery, Columbia Asia Hospital, Ahmedabad, Gujarat, India
EJMO 2018, 2(3), 173–175; https://doi.org/10.14744/ejmo.2018.14632
Submitted: 12 January 2018 | Accepted: 10 February 2018 | Published: 5 May 2018
© 2018 by the Author(s). This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution -Noncommercial 4.0 International License (CC-by the license) ( https://creativecommons.org/licenses/by-nc/4.0/ )
Abstract

Castleman's disease is a rare, benign, lymphoproliferative disorder of unknown cause.[1] The disease can be occasionally associated with a paraneoplastic pemphigus (PNP), an autoimmune mucocutaneous disorder commonly seen in neoplasms of lymphocytic origin.[2] Castleman's tumor has been found in only 10 % of PNP patients,[3] so the diagnosis depends mainly on the pathological examination. For pathological examination, complete surgical excision biopsy of uni-centric disease remains best mode of treatment. We report a case of retrospectively diagnosed case of castleman’s disease with PNP after pathological examination. 

Keywords
Castleman's disease
paraneoplastic pemphigus (PNP)
histopathological examination.
Conflict of interest
None declared.
References

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Eurasian Journal of Medicine and Oncology, Electronic ISSN: 2587-196X Print ISSN: 2587-2400, Published by AccScience Publishing