Hairy Cell Leukemia Presenting with Isolated Skeletal Involvement Successfully Treated by Radiation Therapy and Cladribine: A Case Report and Review of the Literature

Author:

Yonal-Hindilerden Ipek1,Hindilerden Fehmi2,Bulut-Dereli Sanem3,Yıldız Eren4,Dogan Ibrahim Oner5,Nalcaci Meliha1

Affiliation:

1. Istanbul Medical Faculty, Department of Internal Medicine, Division of Hematology, Istanbul University, 34104 Istanbul, Turkey

2. Hematology Clinic, Bakırkoy Sadi Konuk Training and Research Hospital, 34147 Istanbul, Turkey

3. Department of Radiology, Istanbul Bilim University, 34394 Istanbul, Turkey

4. Istanbul Medical Faculty, Department of Orthopaedics and Traumatology, Istanbul University, 34104 Istanbul, Turkey

5. Istanbul Medical Faculty, Department of Pathology, Istanbul University, 34104 Istanbul, Turkey

Abstract

We describe an unusual case of hairy cell leukemia (HCL) in a 55-year-old male presenting with isolated skeletal disease as the initial manifestation without abnormal peripheral blood counts, bone marrow involvement, or splenomegaly. To the best of our knowledge, there have been only two previous reports of a similar case. The patient presented with pain in the right femur. Anteroposterior radiographs of both femurs revealed mixed lytic-sclerotic lesions. PET scan showed multiple metastatic lesions on axial skeleton, pelvis, and both femurs. Histopathological examination of the bone biopsy revealed an infiltrate of HCL. Localized radiation therapy to both proximal femurs and subsequently 4 weeks later, a 7-day course of 0.1 mg/kg/day cladribine provided complete remission with relief of symptoms and resolution of bone lesions. We addressed the manifestations and management of HCL patients with skeletal involvement.

Publisher

Hindawi Limited

Subject

Cell Biology,Developmental Biology,Embryology,Anatomy

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