1 Department of Anatomical Pathology Faculty of Medicine, Sriwijaya University, Palembang, Indonesia
Abstract
Background: Castleman’s disease (CD) is a rare lymphoproliferative disorder that now
bears his name, also known as angiofollicular or giant lymph node hyperplasia. It usually appears in young adult and rarely occurs in chillhood and even rarer in infants and toodler. The disease can be localized or generalized, lymphoproliferative disorder with a frequent mediastinal location, but possible in any lymph node or extra nodal site. Case description : A 10 year old female patient, admitted to RSMH Palembang presented with a mesenterium mass lymph node. Macroscopic appearance reveal smooth to rough two masses measuring 2,5x1x1 cm and 1x1x0,5 cm. Cut section shows a solid, white and encapsulated nodules. Microscopic examination demonstrates lymp nodes with thick fibrocollagen capsule, many lymphoid follicles are atrophy and spread throughout the cortex and medula. Sclerotic blood vessels penetrate the germinal centers forming hyaline vascular lesions similar to “lollipop lesion”. Some foci of residual germinal center contain pink cytoplasmic material, also present in larger germinal center. Some of the follicles are surrounded by a broad mantle zone composed of concentric rings of small lymphocytes like “onion skin”. Interfolicular stroma areas are infiltrated by numerous plasma cells. Immunohistochemical staining using CD 138 highlights plasma cells and BCl2 demarcates the mantle zones. Discussion and conclusion: This case shows accumulated immunoglobulin like pink material, but staining for immunoglobulin was not performed. Based on histopathologic features and immunohistochemical staining, we diagnosed this case as castleman lymphadenopathy myxed hyaline vascular and plasma cell variant type with possible immunoglobulin related disease.