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Castleman's disease of the mesocolon: a rare case report

Mythri Mahesh Boovalli 1
Kalyani Raju 2, *
Srinivas Murthy Venkataramappa 1
  1. Deparment of Pathology, ESIC Medical College & PGIMSR, Rajajonagar, Bangalore, Karnataka, India
  2. ESIC Medical College & PGIMSR, Bangalore, India
Correspondence to: Kalyani Raju, ESIC Medical College & PGIMSR, Bangalore, India. Email: pvphuc@hcmuns.edu.vn.
Volume & Issue: Vol. 1 No. 03 (2014) | Page No.: 93-97 |
Published: 2014-07-24

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This article is published with open access by BioMedPress. This article is distributed under the terms of the Creative Commons Attribution License (CC-BY 4.0) which permits any use, distribution, and reproduction in any medium, provided the original author(s) and the source are credited. 

Abstract

Castleman’s disease is a rare form of localized lymph node hyperplasia of unknown etiology. The sub-types are; hyaline vascular, plasma cell and mixed variant. Clinical subtypes are localized (unicentric) and multicentric. It is reported in all age groups regardless of gender. Hyaline vascular type, accounts for 90% of all cases, often develops in the neck, mediastinum and pulmonary hilum. Its occurrence in the peritoneal cavity is very rare. We present a case in mesocolon of hyaline type in a 39 year female. 

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