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BMC Women s Health· 2026Q1· Case report

Diffuse uterine leiomyomatosis with a mesenteric smooth muscle lesion and a reported family history of uterine leiomyomas: a case report and literature review

Yanping Yu, Qian Chen, Anmei Yao, Yuan Guo et al.

Short summary

A 34-year-old woman with diffuse uterine leiomyomatosis (DUL) developed a similar benign smooth muscle lesion in her mesentery 22 months after initial myomectomy, suggesting recurrent DUL can present with extrauterine lesions.

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Key points

  • Diffuse uterine leiomyomatosis (DUL) is a rare benign smooth muscle disorder characterized by diffuse myometrial nodules.
  • The patient presented with menorrhagia and dysmenorrhea, initially diagnosed as multiple uterine fibroids.
  • Recurrent uterine disease 22 months later was accompanied by a solitary mesenteric nodule, confirmed as a benign smooth muscle lesion similar to DUL.
  • Whole-exome sequencing identified candidate variants in uterine tumor tissue and blood samples.
  • Extrauterine smooth muscle lesions in DUL patients are exceptionally uncommon, and the significance of familial history remains uncertain.

AI-generated from the title and abstract; the full text is not read.

Abstract

Abstract Background Diffuse uterine leiomyomatosis (DUL) is a rare benign smooth muscle disorder characterized by diffuse proliferation of innumerable, poorly circumscribed leiomyomatous nodules throughout the myometrium. Because its clinical and radiologic features overlap with those of multiple conventional uterine leiomyomas, DUL is frequently difficult to diagnose before surgery. Coexisting extrauterine smooth muscle lesions are exceptionally uncommon, and the potential contribution of familial susceptibility to uterine smooth muscle proliferation remains poorly understood. Case presentation We report a 34-year-old woman who presented with progressive menorrhagia and dysmenorrhea and was initially diagnosed with multiple uterine fibroids. She reported a maternal family history of uterine leiomyomas. Myomectomy revealed diffuse, ill-defined nodular smooth muscle proliferation throughout the myometrium, consistent with DUL. Twenty-two months later, recurrent uterine disease required further surgery, aduring which a solitary mesenteric nodule was identified. The patient underwent total hysterectomy and resection of the mesenteric lesion. Histopathological examination confirmed recurrent DUL and a benign mesenteric smooth muscle lesion that was morphologically similar to the uterine lesions. Whole-exome sequencing of the available uterine tumor tissue and blood samples identified candidate variants. A focused review of previously reported cases showed that extrauterine smooth muscle lesions in patients with DUL are rare and that the biological significance of the reported family history remains uncertain. Conclusion This case illustrates that recurrent DUL can coexist with a histologically benign mesenteric smooth muscle lesion and a reported family history of uterine leiomyomas. It highlights the value of integrated clinicopathological assessment and longitudinal follow-up when unusual extrauterine smooth muscle lesions are encountered in patients with DUL.

The authors' abstract, as published at the source. BMC Women s Health, 2026 · DOI ↗

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Field: Obstetrics and Gynecology

Obstetrics and GynecologyMedicine