Syncytial Variant Nodular Sclerosis Classical Hodgkin Lymphoma in an Adolescent and Review of the Literature: A Unique Entity

被引:1
|
作者
Al-Antary, Eman [1 ]
Jesudas, Rohith [1 ,2 ]
George, Amy [1 ,2 ]
Poulik, Janet [3 ]
Savasan, Suereyya [1 ,2 ,4 ]
机构
[1] Childrens Hosp Michigan, Carman & Ann Adams Dept Pediat, Detroit, MI 48201 USA
[2] Wayne State Univ, Sch Med, Div Hematol Oncol, Detroit, MI USA
[3] Wayne State Univ, Sch Med, Dept Pathol, Detroit, MI 48201 USA
[4] Wayne State Univ, Sch Med, Barbara Ann Karmanos Canc Ctr, Pediat Blood & Marrow Transplant Program, Detroit, MI USA
关键词
Hodgkin lymphoma; syncytial variant nodular sclerosis subtype; chest wall bone involvement; neutrophil emperipolesis by Reed-Sternberg-like cells; REED-STERNBERG CELLS; BONE-MARROW ASPIRATE; PATIENT;
D O I
10.1097/MPH.0000000000001245
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Syncytial variant of nodular sclerosis (SV-NS) classical Hodgkin lymphoma (cHL) with its histologic features and clinical presentation is uncommon in adults and extremely rare in children. Here, we report a female teenager presenting with long-standing B symptoms, prominent soft tissue and bone involvement mimicking sarcoma and significant nodal disease who is diagnosed with advanced SV-NS cHL. Rare Reed-Sternberg-like cells displaying neutrophil and erythrocyte emperipolesis were seen on bone marrow aspiration slides. Despite initial complete response to chemotherapy and radiotherapy, the patient experienced early relapse suggestive of high-risk biology. This variant may constitute a unique entity.
引用
收藏
页码:E167 / E170
页数:4
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