Famotidine-induced reactive plasmacytosis and generalized lymphadenopathy: a case report and review of the literature
نویسندگان
چکیده
We report the case of a 53-year-old woman who presented with plasmacytosis, hypergammaglobulinemia, and multiple lymphadenopathy after upper respiratory infection. Although these symptoms mimicked those of plasma cell leukemia, serum immunoelectrophoresis, flow cytometry, and immunohistochemistry of bone marrow and an enlarged lymph node revealed polyclonal proliferation of plasma cells. In the absence of treatment, the plasmacytosis improved soon after ceasing the previously prescribed medications. A drug reaction was suspected as the cause of plasmacytosis because the patient had high serum IgE levels that decreased after discontinuation of the medications. A drug-induced lymphocyte stimulation test was performed for all of the drugs prescribed before admission: a positive result was only obtained for famotidine. The present case represents the first report of marked famotidine-associated plasmacytosis.
منابع مشابه
Rosai-Dorfman Disease: A Case Report and Literature Review
Rosai-Dorfman disease or sinus histiocytosis with massive lymphadenopathy is a rare disorder that typically manifests as lymphadenopathy and systemic symptoms whose etiology remains poorly elucidated. The diagnosis is based on immunohistochemistry. Its treatment is poorly defined but the prognosis is usually favorable. Here we report a 14 year old boy who presented with massive bilateral cervi...
متن کاملACNE FULMINANS ASSOCIATED WITH REACTIVE POLYARTHRITIS: REPORT OF A CASE AND REVIEW OF THE LITERATURE
We describe a 16 year old boy with acne fulminans associated with axial and peripheral polyarthritis. The patient's clinical course and therapy with isotretinoin, prednisolone and oxytetracycline are described. A possible association between the presence of HLA -B 27 antigen and reactive arthritis with acne fulminans in this case is evaluated. A review of the literature is included.
متن کاملUnilateral generalized morphea: A case report and literature review
Morphea is an autoimmune connective tissue disease of the dermis and subcutaneous fat characterized by sclerosis due to excessive collagen deposition. Morphea is classified into different subtypes based on clinical and histological characteristics of cutaneous lesions. An extremely rare subtype of morphea is termed unilateral generalized morphea (UGM). UGM is characterized by indurated plaques ...
متن کاملMALIGNANT HISTIOCYTOSIS: A CASE REPORT AND REVIEW OF THE LITERATURE
Malignant histiocytosis (MH) is a rare hematologic malignancy, especially in the first decade of life. The disease is clinically characterized by fever, hepatosplenomegaly, lymphadenopathy, pancytopenia and jaundice, and histologically by systemic proliferation of malignant histiocytes and hemophagocytosis. The prognosis is poor and often the diagnosis is not made before death. Because of ...
متن کاملA Huge Lymphangioma Mimicking Pleural Effusion with Extension to Both Chest Cavities: A Case Report and Review of Literature
Mediastinal lymphangioma is primarily a benign lesion and the majority of the cases are found incidentally. These lesions account for approximately 1% of all mediastinal tumors. Here we present a giant mediastinal cystic mass in a 35-year-old female who was presented with severe respiratory distress. On the plain chest radiography and CT scan, a massive left pleural effusion with large paraster...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
عنوان ژورنال:
دوره شماره
صفحات -
تاریخ انتشار 2016