Krishnan Amit, Schmoke Nicholas, Nemeh Christopher, Wu Yeu Sanz, Duron Vincent
Westchester Medical Center, School of Medicine, New York Medical College, Valhalla, NY 10595, United States.
Division of Pediatric Surgery, Department of Surgery, Columbia University Vagelos College of Physicians and Surgeons/New York-Presbyterian Morgan Stanley Children's Hospital, New York, NY 10032, United States.
J Surg Case Rep. 2023 Sep 15;2023(9):rjad502. doi: 10.1093/jscr/rjad502. eCollection 2023 Sep.
A congenital pulmonary airway malformation (CPAM) occurring concurrently with an enteric duplication cyst is a rare anomaly. Definitive management for both abnormalities is usually surgical resection. We present the uncommon case of a neonate with a CPAM and ileal duplication cyst, including pre-natal and post-natal workup. The patient was brought to the operating room for laparoscopic duplication cyst excision at 3 months of age. The patient returned to the operating room for a thoracoscopic right lower lobectomy at five months of age. This case presents a rare congenital anomaly with the concurrent presentation of a CPAM and enteric duplication cyst, with both being successfully excised minimally invasively.
先天性肺气道畸形（CPAM）与肠道重复囊肿同时出现是一种罕见的异常情况。对这两种异常情况的明确治疗通常是手术切除。我们报告了一例患有CPAM和回肠重复囊肿的新生儿的罕见病例，包括产前和产后检查。该患者在3个月大时被送往手术室进行腹腔镜下重复囊肿切除术。患者在5个月大时再次回到手术室进行胸腔镜右下叶切除术。本病例呈现了一种罕见的先天性异常，即CPAM和肠道重复囊肿同时出现，且两者均通过微创手术成功切除。
