Iraqi Journal of Hematology

CASE REPORT
Year
: 2018  |  Volume : 7  |  Issue : 1  |  Page : 45--47

Management of a patient with Rosai–Dorfman syndrome and large adrenal pheochromocytoma


Taha O Mahwi1, Najmaddin Khoshnaw2 
1 Department of Medicine, Faculty of Medicine, School of Medicine, University of Sulaimani, Sulaymaniyah, Iraq
2 Department of Haematology, Hiwa Hospital, Sulaymaniyah; Department of Haematology, Kurdistan Board for Medical Specialties, Ministry of Higher Education and Scientific Research, Erbil, Iraq

Correspondence Address:
Dr. Najmaddin Khoshnaw
Department of Haematology, Hiwa Hospital, PO. Box: 54 at Al-Sulaymaniyah Post Office, Sulaymaniyah, Kurdistan Region
Iraq

Sinus histiocytosis with massive lymphadenopathy that known as Rosai Dorfman syndrome (RDS)is a rare histiocytic disease which includes benign lymph nodes (LN) enlargement with extra-lymphatic soft tissue involvement. The concomitant presentation of RDS with an adrenal tumor is rarely encountered among our patients. Here in we describe a middle-aged man, presented with a chronic history of repeated LN enlargement. The nodes had mild local discomfort and tenderness with associated fever. LN biopsy showed sinus histiocytosis with lymphophagocytosis characterized as emperipolesis and diagnosis of RDS was decided. After one year, the patient presented with high blood pressure, raised blood sugar, obesity, and abdominal pain. Computerized tomography showed a large adrenal mass, and the patient was treated urgently for his malignant blood pressure followed by surgical excision of the left adrenal mass. The biopsy subsequently revealed non-malignant adrenal tumor (pheochromocytoma). We are reporting successful treatment of rare case with RDS concomitantly presented with large adrenal pheochromocytoma. He was treated medically and surgically, the patient got recovery. RDS is a rare disease but we should consider it in patients with repeated benign lymphadenopathy. we are emphasizing that knowledge about RDS and its disease associations may be informative to the general medical community.


How to cite this article:
Mahwi TO, Khoshnaw N. Management of a patient with Rosai–Dorfman syndrome and large adrenal pheochromocytoma.Iraqi J Hematol 2018;7:45-47


How to cite this URL:
Mahwi TO, Khoshnaw N. Management of a patient with Rosai–Dorfman syndrome and large adrenal pheochromocytoma. Iraqi J Hematol [serial online] 2018 [cited 2022 Jun 25 ];7:45-47
Available from: https://www.ijhonline.org/article.asp?issn=2072-8069;year=2018;volume=7;issue=1;spage=45;epage=47;aulast=Mahwi;type=0