This case underscores the importance of maintaining clinical suspicion for uterine AML when encountering large or atypical uterine lesions and enrichs the understanding of extrarenal AMLs in gynecologic practice.
Abstract
ABSTRACT Background Angiomyolipoma (AML) is a rare benign mesenchymal tumor, originating from perivascular epithelioid cells (PECs), composed of smooth muscle, fat, and thick-walled blood vessels, most often found in the kidney. Uterine AML is exceptionally rare, with under 40 cases reported worldwide and 3 from India prior to the present case. Unlike renal AMLs, uterine lesions are typically sporadic and not linked to tuberous sclerosis (TS), which, combined with their resemblance to fibroids, makes preoperative diagnosis challenging. Case Description A 49-year-old woman presented with six months of progressive lower abdominal distension and three months of amenorrhea. She had no signs of TS. Physical examination revealed a firm, non-mobile pelvic mass extending to the xiphisternum. Contrast-enhanced Computed Tomography (CT) showed a 27 × 18 × 19 cm submucosal uterine mass with right hydroureteronephrosis; Cancer Antigen-125 (CA 125 ag) was normal. A total abdominal hysterectomy with bilateral salpingo-oophorectomy was performed, revealing a 7 kg anterior wall tumor. Histopathology confirmed classic AML architecture—interlacing smooth muscle bundles, mature adipocytes, and hyalinized blood vessels—without atypia or mitotic activity. She recovered well. Discussion Uterine AML is a “diagnostic chameleon,” often mistaken for leiomyomas, lipoleiomyomas, or degenerated fibroids on imaging. Definitive diagnosis relies on histopathological examination. Each reported case contributes vital insights into this rare gynecologic entity and highlights the need to include AML in the differential diagnosis of unusual uterine masses. Conclusion This case underscores the importance of maintaining clinical suspicion for uterine AML when encountering large or atypical uterine lesions. Our patient underwent a hysterectomy and had an uneventful recovery. Histologic confirmation and complete surgical excision are key to optimal management and favorable outcomes, enriching our understanding of extrarenal AMLs in gynecologic practice.
Angiolipoleiomyoma (ALLM) is a rare benign mesenchymal tumor that primarily arises in the skin and kidney, and less frequently in the uterus. The present case may represent the largest reported uterine mass described as ALLM. We present a case of a 52‐year‐old woman with abdominal fullness and an irregular menstrual cy...
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Background: Extra-uterine leiomyomatosis is a rare benign condition characterized by the proliferation of smooth muscle cells outside the uterus. Its clinical presentation is often misleading and may mimic malignant pelvic disease, particularly in patients with a history of uterine surgery. Case presentation: We report...
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This case highlights the importance of considering Müllerian anomalies when pelvic examination and imaging findings do not completely explain the anatomy, and careful preoperative assessment and anticipation of altered pelvic anatomy are important for safe surgical management of large leiomyomas associated with uterine...
S. Dave, Mahima Jain· International Journal of Rep...· 0 citations
Ovarian myxoma is a rare benign mesenchymal tumor. It can be completely asymptomatic and is difficult to differentiate from other ovarian masses before surgery and final histopathology. We report a case of a 28-year-old primigravida who presented with a missed abortion at 11 weeks. Transvaginal ultrasonography incident...