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阑尾黏液性囊腺癌合并自发性皮肤瘘

[Mucinous cystadenocarcinoma of the appendix complicated with spontaneous cutaneous fistula].

作者信息

Ghidirim G, Gagauz I, Mişin I, Canariov M, Ionesii P, Zastavnitchi G

机构信息

Catedra Chirurgie nr. 1 N. Anestiadi şi Laboratorul de Chirurgie Hepato-Bilio-Pancreatică, Universitatea de Medicină şi Farmacie N. Testemiţanu, Spitalul Clinic Municipal de Urgenţă, Chişinău, Moldova.

出版信息

Chirurgia (Bucur). 2007 Mar-Apr;102(2):231-5.

Abstract

Mucocele of the appendix is a relatively rare disease characterized by a cystic dilatation of the appendiceal lumen with stasis of mucus inside. Appendiceal mucocele with a cutaneous fistula is an extremely rare clinical entity, only four such cases being described in the medical literature. We report an additional case of cystadenocarcinoma of the appendix with spontaneous cutaneous fistula. The patient is an 80-year old woman, who originally presented with a skin ulcer in the right lower abdominal quadrant with mucus discharge during the last month. Abdominal ultrasonography and computed tomography demonstrated cystic mass with mixed echogenity and density originating from the appendix, involving the abdominal wall, without signs of ascites or metastasis. A right hemi-colectomy, lymphadenectomy and resection of the skin fistula was performed. The histological findings revealed moderately differentiated mucinous cystadenocarcinoma of the appendix. The postoperative period was uneventful and the patient discharged on the 11th POD. During 12 month follow-up period the patient is free of disease recurrence. The authors present the literature review, diagnostic features and the treatment policy of this extremely rare condition.

摘要

阑尾黏液囊肿是一种相对罕见的疾病,其特征为阑尾腔呈囊性扩张且内部黏液淤滞。伴有皮肤瘘管的阑尾黏液囊肿是一种极其罕见的临床病症,医学文献中仅描述过4例此类病例。我们报告1例伴有自发性皮肤瘘管的阑尾囊腺癌病例。患者为一名80岁女性,最初表现为右下腹象限皮肤溃疡,近1个月有黏液排出。腹部超声和计算机断层扫描显示,起源于阑尾的囊实性肿物,累及腹壁,无腹水或转移迹象。实施了右半结肠切除术、淋巴结清扫术及皮肤瘘管切除术。组织学检查结果显示为阑尾中度分化黏液性囊腺癌。术后恢复顺利,患者于术后第11天出院。在12个月的随访期内,患者无疾病复发。作者介绍了这种极其罕见病症的文献综述、诊断特征及治疗策略。

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