Fox Kristen E, Philip Dwight, Motta Monique, Ansari-Lari M Ali, Levene Tamar L
Medicine, Herbert Wertheim College of Medicine, Miami, USA.
Pediatrics, Joe DiMaggio Children's Hospital, Hollywood, USA.
Cureus. 2024 Aug 18;16(8):e67131. doi: 10.7759/cureus.67131. eCollection 2024 Aug.
B-cell lymphoblastic lymphoma (B-LBL) is a subtype of non-Hodgkin lymphoma characterized by the proliferation of abnormal B-cell lymphoblasts in lymphoid tissues. Typical presentations include lymphadenopathy, mediastinal mass, and involvement of organs such as the liver and spleen, but extranodal sites can also be affected. A previously healthy 20-month-old male child presented to the pediatric surgery clinic with a two-month history of a painless, progressively enlarging mass on the scalp as well as postauricular mass consistent with an enlarged lymph node. Ultrasound of the mass near the vertex demonstrated a hypoechoic complex cystic lesion for which excision was indicated. Preoperatively, acute enlargement of the entire postauricular lymphatic chain was noted. Intraoperatively, the scalp mass was noted to be firm with calcified tissue and no identifiable cystic or infectious components. The mass and part of the overlying skin were excised. Pathologic evaluation was consistent with B-LBL. The patient was therefore referred to a pediatric oncologist for further evaluation and management. Bone marrow examination revealed greater than 25% blasts in the clot section, consistent with B-ALL. He was promptly initiated on induction therapy with maintenance chemotherapy to ensure continued remission. This case highlights the atypical presentation of B-cell lymphoblastic leukemia/lymphoma (B-ALL/LBL) as a scalp mass in a 20-month-old male. It underscores the importance of considering malignancy in the differential diagnosis of unusual masses. Prompt collaboration between pediatric surgeons and oncologists facilitates timely diagnosis and initiation of appropriate treatments for optimal outcomes.
B细胞淋巴母细胞淋巴瘤(B-LBL)是非霍奇金淋巴瘤的一种亚型,其特征是异常B细胞淋巴母细胞在淋巴组织中增殖。典型表现包括淋巴结病、纵隔肿块以及肝脏和脾脏等器官受累,但结外部位也可能受到影响。一名此前健康的20个月大男童因头皮上有一个无痛性、逐渐增大的肿块以及耳后肿块(与肿大的淋巴结一致),持续两个月,前往小儿外科诊所就诊。头顶附近肿块的超声检查显示为低回声复合囊性病变,需要进行切除。术前,发现整个耳后淋巴链急性肿大。术中,发现头皮肿块质地坚硬,有钙化组织,没有可识别的囊性或感染性成分。切除了肿块及部分覆盖皮肤。病理评估与B-LBL一致。因此,该患者被转诊至小儿肿瘤学家处进行进一步评估和治疗。骨髓检查显示凝块切片中原始细胞超过25%,与B-ALL一致。他立即开始接受诱导治疗及维持化疗,以确保持续缓解。该病例突出了B细胞淋巴母细胞白血病/淋巴瘤(B-ALL/LBL)在一名20个月大男性中表现为头皮肿块的非典型情况。它强调了在不寻常肿块的鉴别诊断中考虑恶性肿瘤的重要性。小儿外科医生和肿瘤学家之间的及时合作有助于及时诊断并启动适当治疗,以实现最佳治疗效果。