Lymphangiome kystique du mésocolon: à propos d’un cas.

IF 0.9 Q4 PUBLIC, ENVIRONMENTAL & OCCUPATIONAL HEALTH
Pan African Medical Journal Pub Date : 2024-08-02 eCollection Date: 2024-01-01 DOI:10.11604/pamj.2024.48.144.35940
Abdelkrim Chetibi, Kamel Allal, Mustapha Saidani
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引用次数: 0

Abstract

Intraperitoneal Cystic Lymphangioma (CL) is a rare benign malformative disease of lymphatic origin, with a wide range of clinical symptoms. Diagnosis is based on imaging tests and confirmed by histology. We here report the case of a 54-year-old woman presenting with chronic abdominal pain, with no effect on general condition. Radiological assessment showed a benign mesenteric cystic formation consistent with a cystic lymphangioma. Complete surgical excision of the cystic mass after puncture-aspiration was performed via midline laparotomy, with an uncomplicated postoperative course. Histological examination of the lumpectomy confirmed the diagnosis of LK of the mesocolon. At 12 months, the patient was asymptomatic and no recurrence was observed.

结肠系膜囊性淋巴管瘤:病例报告。
腹膜内囊性淋巴管瘤(CL)是一种罕见的淋巴源性良性畸形疾病,具有多种临床症状。诊断依据是影像学检查和组织学确诊。我们在此报告了一例 54 岁女性的病例,她出现慢性腹痛,但对全身状况没有影响。放射学评估显示其肠系膜良性囊肿与囊性淋巴管瘤一致。经中线腹腔镜穿刺抽吸后,对囊性肿块进行了完整的手术切除,术后并无并发症。肿块切除后的组织学检查证实了结肠系膜淋巴结核的诊断。12 个月后,患者无任何症状,也未发现复发。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Pan African Medical Journal
Pan African Medical Journal PUBLIC, ENVIRONMENTAL & OCCUPATIONAL HEALTH-
CiteScore
1.80
自引率
0.00%
发文量
691
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