A rare case of Richter transformation with breast involvement: A case report and literature review

Author:

Wang Wenhui1,Chen Hao1,Ju Wendong2,Yang Weihong3,Ding Gaoming2,Wang Li4

Affiliation:

1. Department of Pathology, Hangzhou Women’s Hospital , Hangzhou , Zhejiang , China

2. Department of Oncology and Hematology, Zhongshan Boai Hospital Affiliated to Southern Medical University , Zhongshan 528403, Guangdong , China

3. Department of Pathology, Zhongshan Boai Hospital Affiliated to Southern Medical University, Zhongshan , Guangdong , China

4. Department of Oncology and Hematology, Zhongshan Boai Hospital Affiliated to Southern Medical University , 6 Chenggui Road, East District , Zhongshan , 528403, Guangdong , China

Abstract

Abstract Richter transformation (RT) represents the development of intrusive lymphoma in individuals previously or concurrently diagnosed with chronic lymphocytic leukemia (CLL) and is characterized by lymph node enlargement. However, cases involving extra-nodal organ involvement as the first symptom are rare. There are no reports of RT with breast lesions as the first symptom. Nonspecific and atypical clinical manifestations represent key challenges in the accurate diagnosis and appropriate treatment of RT. This case report describes an elderly female patient who presented with breast lesions as the first RT symptom. The patient was admitted with a painless mass in the left breast. Examination revealed multiple lymphadenopathies and abnormally high white blood cell levels. The patient was diagnosed with CLL after hematological tests, assessments of bone marrow morphology, and tissue biopsy. Mammography and B-ultrasonography showed solid space-occupying lesions (BI-RADS category 5) in the left breast. Initially, the patient declined a breast biopsy and was therefore prescribed ibrupotinib treatment, which showed limited efficacy. A needle biopsy of the affected breast indicated the presence of diffuse large B-cell lymphoma. Based on auxiliary and pathological examinations and medical history, the final diagnosis was RT with breast involvement. Zanubrutinib with rituximab, cyclophosphamide, doxorubicin, vincristine, and prednisone treatment provided initial control; however, the treatment strategy required adjustment because of the patient’s fluctuating condition. The current status of the patient is marked as stable, showing an overall achievement of partial alleviation. The patient is in the process of receiving follow-up treatment. We also performed a comprehensive literature review on RT, with particular emphasis on its biological paradigm, prognosis implications, existing therapeutic approaches, and emerging directions in treatment modalities.

Publisher

Walter de Gruyter GmbH

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