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Rosai-Dorfman disease involving gallbladder and liver-Report of a case
Elena Arabadzhieva1, Atanas Yonkov1, Sasho Bonev1
1Department of General and Hepato-Pancreatic Surgery, University Hospital "Alexandrovska" - Sofia, Medical University - Sofia, 1 G.Sofiiski Str., 1431 Sofia, Bulgaria.
Introduction:
Rosai-Dorfman disease (RDD), also known as sinus histiocytosis with massive lymphadenopathy, is a rare histiocytic disorder of unclear etiology. Lymphadenopathy commonly affects the lymph nodes of the neck and the head, but extranodal involvement has been observed too.
Presentation Of Case:
We describe an unusual case of RDD with involvement of the gallbladder, liver and cystic lymph node, clinically manifested as an exacerbated cholecystitis. The patient underwent a cholecystectomy with atypical liver resection because the finding was macroscopically suspected of gallbladder cancer. The diagnosis of RDD was confirmed by immunohistochemical study.
Discussion:
Histological features of RDD include histiocytic proliferation, emperipolesis and positive immunostaining for S-100 protein and typically negative for CD1a. Gastrointestinal localization of RDD, especially in the liver and pancreas, is extremely rare. Typically, the liver is affected as a part of systematic spread of RDD. We have not found reports for involvement of the gallbladder.
Conclusion:
The presented case is valuable due to its rarity and difficulty in differential diagnosis.
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