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急诊脾切除术后偶然诊断为腹膜假黏液瘤。

Incidental Diagnosis of Pseudomyxoma Peritonei After Emergent Splenectomy.

机构信息

Department of General Surgery, Digestive Disease and Surgery Institute, Cleveland Clinic, OH, USA.

Division of General Surgery/Division of Surgical Oncology, Department of Surgery, MetroHealth System, OH, USA.

出版信息

Am Surg. 2023 Apr;89(4):1115-1117. doi: 10.1177/0003134820954822. Epub 2020 Dec 19.

Abstract

Pseudomyxoma peritonei (PMP) is a rare disease associated with mucinous ascites. Pseudomyxoma peritonei has a low incidence and is difficult to diagnose. Pseudomyxoma peritonei usually presents with vague abdominal pain after significant progression. Computed tomography imaging is the most common modality for diagnosis; however, diagnosis as a result of surgical intervention in cases of acute abdomen has become increasingly common. We present a unique case of a 66-year-old man who was incidentally diagnosed with PMP after undergoing an emergent splenectomy for presumed blunt trauma. The patient presented to the emergency room with abdominal pain, shortness of breath, and diaphoresis. Computed tomography imaging revealed a splenic hematoma with suspicion of extravasation and a moderate amount of free intraperitoneal fluid consistent with blood. The patient was taken to the operating room emergently for an emergent splenectomy where splenic laceration was noted, as were multiple areas of nodularity in the omentum and cecum. Histologic evaluation of these lesions led to the diagnosis of PMP. After recovery from his initial splenectomy, the patient underwent exploratory laparotomy, cytoreductive surgery, cholecystectomy, removal of appendiceal mucocele, and hyperthermic intraperitoneal chemotherapy without complication. Final pathology was consistent with PMP and primary mucinous appendiceal adenocarcinoma. This case highlights an unusual presentation of PMP for a patient who was undergoing surgery for presumed splenic trauma. Surgeons must maintain a high index of suspicion and should perform histological evaluation when such unexpected findings are encountered.

摘要

腹膜假性黏液瘤(PMP)是一种与黏液性腹水相关的罕见疾病。腹膜假性黏液瘤发病率低,诊断困难。腹膜假性黏液瘤通常在明显进展后出现模糊的腹痛。计算机断层扫描成像(CT)是最常见的诊断方式;然而,由于急性腹痛进行手术干预的诊断变得越来越常见。我们报告了一个独特的病例,一名 66 岁男性因疑似钝性创伤而行紧急脾切除术时意外诊断为 PMP。该患者因腹痛、呼吸急促和出汗到急诊就诊。CT 成像显示脾血肿伴外渗可疑,并有中等量的游离腹腔积液,符合血液。患者紧急被送往手术室进行紧急脾切除术,术中发现脾裂伤,并在大网膜和盲肠多处有小结节。这些病变的组织学评估导致了 PMP 的诊断。在最初的脾切除术后恢复后,患者接受了探查性剖腹手术、细胞减灭术、胆囊切除术、阑尾黏液囊肿切除术和腹腔内热化疗,无并发症。最终的病理结果与 PMP 和原发性黏液性阑尾腺癌一致。这个病例突出了 PMP 对接受疑似脾损伤手术的患者的不常见表现。外科医生必须保持高度的怀疑指数,如果遇到这种意外的发现,应进行组织学评估。

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