Millot F, Klossek J M, Brizard F, Brizard A, Vandermarq P, Babin P, Guilhot F
Department of Hematology and Medical Oncology, Hospital J. Bernard, Poitiers, France.
J Pediatr Hematol Oncol. 1997 Jul-Aug;19(4):351-3. doi: 10.1097/00043426-199707000-00016.
Extramedullary relapse of childhood acute lymphoblastic leukemia most commonly occurs in the central nervous system or in the testes. Otologic involvement is very rare and has only been reported as an autopsy finding.
We describe the case of a 5-year-old girl with CD10 positive acute lymphoblastic leukemia (ALL) who developed an isolated otologic relapse 18 months after the initial diagnosis of ALL.
This otologic relapse presented as an atypical otitis media related to a mass of the middle ear. The leukemic infiltration of the middle ear was demonstrated by histologic examination. A cytogenetic change characterized by the occurrence of t(1;19)(q23;p13) was observed in the leukemic cells from the middle ear, and the t(1;19) molecular fusion transcript E2A-PBX1 was detected in the bone marrow by polymerase chain reaction.
The ear is an exceedingly rare site of relapse in children with acute lymphoblastic leukemia. Molecular analysis demonstrates that such an extramedullary relapse can represent an early manifestation of systemic relapse.
儿童急性淋巴细胞白血病的髓外复发最常发生于中枢神经系统或睾丸。耳部受累极为罕见,仅有尸检报告。
我们描述了一名5岁CD10阳性急性淋巴细胞白血病(ALL)女孩的病例,该患儿在ALL初诊18个月后出现孤立性耳部复发。
此次耳部复发表现为与中耳肿物相关的非典型中耳炎。组织学检查证实中耳有白血病浸润。在中耳白血病细胞中观察到以t(1;19)(q23;p13)出现为特征的细胞遗传学改变,通过聚合酶链反应在骨髓中检测到t(1;19)分子融合转录本E2A-PBX1。
耳部是急性淋巴细胞白血病患儿极为罕见的复发部位。分子分析表明,这种髓外复发可能是全身复发的早期表现。