Hozaka Yuto, Sasaki Ken, Nishikawa Takuro, Onishi Shun, Noda Masahiro, Tsuruda Yusuke, Uchikado Yasuto, Kita Yoshiaki, Arigami Takaaki, Mori Shinichiro, Maemura Kosei, Ieiri Satoshi, Kawano Yoshifumi, Natsugoe Shoji, Ohtsuka Takao
Department of Digestive Surgery, Breast and Thyroid Surgery, Graduate School of Medical and Dental Sciences, Kagoshima University, 8-35-1 Sakuragaoka, Kagoshima-shi, Kagoshima, 890-8520, Japan.
Department of Pediatrics, Graduate School of Medical and Dental Sciences, Kagoshima University, 8-35-1 Sakuragaoka, Kagoshima-shi, Kagoshima, 890-8520, Japan.
Surg Case Rep. 2021 Feb 5;7(1):41. doi: 10.1186/s40792-021-01108-8.
Anaplastic large cell lymphoma (ALCL) is a CD30-positive T-cell lymphoma, which is a rare type of non-Hodgkin lymphoma. ALCL rarely presents in the gastrointestinal tract, and the esophageal involvement in of ALCL is extremely rare.
An 11-year-old boy who complained of abdominal pain and cough was diagnosed with ALK-positive ALCL on the basis of systemic lymphadenopathy findings and immunohistochemistry results of pleural effusion. Although remission was observed after chemotherapy at 5 months after diagnosis, dysphagia persisted, and esophagoscopy revealed a severe stricture in the middle thoracic esophagus. At 9 months after diagnosis, allogeneic bone marrow transplantation was performed to ensure that complete remission was maintained; however, dysphagia and saliva retention did not improve. Approximately 10 months after diagnosis, esophagoscopy revealed a blind end in the middle thoracic esophagus, similar to that in congenital esophageal atresia. Subsequently, we performed minimally invasive subtotal esophagectomy under thoracoscopy and laparoscopy and gastric conduit reconstruction via the retrosternal route more than 2 years after allogeneic bone marrow transplantation. The final pathological diagnosis was esophageal atresia with esophagitis, with no malignancy. During postoperative evaluation, the patient required swallowing training for a few months, although no major complications were noted. Oral intake was possible, and complete remission was maintained at 14 month post-surgery.
Oncologists must consider the possibility of acquired esophageal cicatricial atresia as a complication during chemotherapy for ALCL. If esophageal obstruction or esophageal atresia occur and if remission is maintained, esophagectomy and esophageal reconstruction are useful treatment options for maintaining oral intake.
间变性大细胞淋巴瘤(ALCL)是一种CD30阳性的T细胞淋巴瘤,是一种罕见的非霍奇金淋巴瘤。ALCL很少出现在胃肠道,食管受累极为罕见。
一名11岁男孩,主诉腹痛和咳嗽,根据全身淋巴结肿大的表现及胸腔积液的免疫组化结果,被诊断为ALK阳性的ALCL。尽管在诊断后5个月化疗后病情缓解,但吞咽困难持续存在,食管镜检查显示胸段食管中段严重狭窄。诊断后9个月,进行了异基因骨髓移植以确保维持完全缓解;然而,吞咽困难和唾液潴留并未改善。诊断后约10个月,食管镜检查显示胸段食管中段呈盲端,类似于先天性食管闭锁。随后,在异基因骨髓移植2年多后,我们通过胸腔镜和腹腔镜进行了微创次全食管切除术,并经胸骨后途径进行了胃代食管重建术。最终病理诊断为食管炎伴食管闭锁,无恶性肿瘤。术后评估期间,患者需要进行数月的吞咽训练,尽管未发现重大并发症。患者能够经口进食,术后14个月维持完全缓解。
肿瘤学家必须考虑获得性食管瘢痕性闭锁作为ALCL化疗期间并发症的可能性。如果发生食管梗阻或食管闭锁且病情维持缓解,食管切除术和食管重建术是维持经口进食的有效治疗选择。