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Leiomyomatosis peritonealis disseminata: a rare disease with a difficult diagnosis
Daniel Martins Jordão1, João Santos Pereira1, Emanuel Furtado2
1Serviço de Cirurgia Geral, Instituto Portugues de Oncologia de Coimbra Francisco Gentil EPE, Coimbra, Portugal.
Abstract:
Leiomyomatosis peritonealis disseminata (LPD) is a rare condition, characterised by the proliferation of peritoneal smooth muscle nodules. LPD is a benign disease with a low rate of malignant degeneration. We describe the case of a 46-year-old, asymptomatic, woman presenting with a mass on the left renal hilum, identified by ultrasound. A CT scan showed three nodules near the left kidney, a mass anterior to the vena cava and bilateral iliac nodules. Biopsy revealed a mesenchymal low-grade tumour. The patient underwent a left nephrectomy and excision of the other masses. The histological diagnosis revealed smooth muscle nodular proliferation with no malignant features, compatible with LPD. The differential diagnosis between LPD and metastatic leiomyosarcoma is sometimes very difficult because they are clinically very similar and even on histology the diagnosis can be tricky. Treatment is conservative in most cases, with surgical excision reserved for high-risk patients.
Insights
Leiomyomatosis peritonealis disseminata (LPD) is a rare condition of smooth muscle nodules. This case highlights diagnostic challenges and the importance of differentiating LPD from leiomyosarcoma, with conservative treatment often preferred.
Area of Science:
- Oncology
- Pathology
- Gastroenterology
Background:
- Leiomyomatosis peritonealis disseminata (LPD) is a rare condition characterized by smooth muscle nodules in the peritoneum.
- LPD is generally benign but can be challenging to differentiate from malignant conditions like leiomyosarcoma.
Observation:
- A 46-year-old asymptomatic woman presented with multiple masses identified via ultrasound and CT scans.
- Imaging revealed nodules near the left kidney, anterior to the vena cava, and in the iliac regions.
Findings:
- Biopsy indicated a low-grade mesenchymal tumor.
- Histological examination confirmed smooth muscle nodular proliferation consistent with LPD, without malignant features.
Implications:
- Distinguishing LPD from metastatic leiomyosarcoma can be challenging due to clinical and histological similarities.
- Conservative management is typical, with surgical excision reserved for high-risk individuals.
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