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一名无手术史女性的维拉结节病例报告。

A case report of Villar's nodule in a woman without surgical history.

作者信息

Ouédraogo Nabonswindé Lamoussa Marie, Ilboudo Safy, Ouattara Abdoul Karim, Ouedraogo Aimé Sosthène, Zida Maurice, Zongo Nayi, Obiri-Yeboah Dorcas, Ouangre Edgard, Simpore Jacques, Traore Si Simon

机构信息

Service of General Surgery of Saint Camille Hospital of Ouagadougou, 01 BP 444 Ouagadougou 01, Burkina Faso.

Gynecology Service of Saint Camille Hospital of Ouagadougou, 01 BP 444 Ouagadougou 01, Burkina Faso.

出版信息

Int J Surg Case Rep. 2018;53:186-188. doi: 10.1016/j.ijscr.2018.10.066. Epub 2018 Nov 1.

Abstract

INTRODUCTION

Villar's nodule is an umbilical endometriosis without anterior or ongoing pelvic endometriosis. The primitive location of this nodule at the umbilical level is rare. Its etiopathogenesis remains unclear.

PRESENTATION OF CASE

We report a case of umbilical endometriosis with unusual clinical expression in a woman in the reproductive years with no surgical history and no known history of endometriosis. Endometriosis manifested as progressive transformation of the normal umbilicus into several small nodules, with bleeding coinciding with the menstrual cycle. The diagnosis was confirmed by histology and surgical treatment consisted of omphalectomy.

DISCUSSION

Umbilical endometriosis is a rare disease that occurs naturally in patients with pelvic endometriosis. Etiopathogenesis of the disease is still unclear. In our patient, the appearance of the nodule was impressively, by a gradual transformation of the normal aspect of the umbilicus, into several small, slightly pigmented, firm, painful and concomitantly bleeding nodules during periods of menstruation. In the literature, this multinodular or budding form would be of exceptional observation.

CONCLUSION

The characteristics of the umbilical tumor, associated with the cyclical nature of tumor bleeding in a patient without previous history of endometriosis, strongly suggest the diagnosis of Villar's nodule, but the confirmation is still histological. The treatment is always surgical and recurrence is very rare.

摘要

引言

维拉尔结节是一种无盆腔前部或进行性子宫内膜异位症的脐部子宫内膜异位症。该结节在脐部水平的原始位置罕见。其发病机制尚不清楚。

病例介绍

我们报告一例生殖期女性的脐部子宫内膜异位症,临床表现不寻常,该女性无手术史且无已知子宫内膜异位症病史。子宫内膜异位症表现为正常脐部逐渐转变为几个小结节,出血与月经周期相符。组织学确诊,手术治疗为脐切除术。

讨论

脐部子宫内膜异位症是一种罕见疾病,自然发生于盆腔子宫内膜异位症患者。该疾病的发病机制仍不清楚。在我们的患者中,结节的出现令人印象深刻,表现为脐部正常外观逐渐转变为几个小的、轻度色素沉着、坚实、疼痛且在月经期间伴有出血的结节。在文献中,这种多结节或芽状形式的观察极为罕见。

结论

脐部肿瘤的特征,与无子宫内膜异位症病史患者肿瘤出血的周期性相关,强烈提示维拉尔结节的诊断,但仍需组织学确诊。治疗始终是手术治疗,复发非常罕见。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0306/6222089/5d7e50c1ea9f/gr1.jpg

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