Pulmonary BML should be considered in the differential diagnosis of multiple pulmonary nodules in women with a remote history of uterine leiomyoma, and mild FDG uptake cannot distinguish pulmonary BML from a low-grade malignancy.
Abstract
Background Benign metastasizing leiomyoma (BML) is a rare smooth-muscle tumor that occurs in patients with a history of uterine leiomyoma, with the lungs being the most commonly involved extrauterine site. Pulmonary BML can mimic metastatic malignancy on imaging. Decades-long intervals after uterine surgery have been reported, and 18F-FDG uptake may vary among lesions. Case presentation A 59-year-old postmenopausal, nonsmoking woman presented with multiple bilateral pulmonary nodules 30 years after hysterectomy for uterine leiomyoma. 18F-FDG PET/CT demonstrated mild FDG uptake in the dominant pulmonary lesion, with a maximum standardized uptake value (SUVmax) of 2.44. Although the uptake was not strongly suggestive of an aggressive malignancy, a low-grade neoplasm could not be excluded. Video-assisted thoracoscopic wedge resection was therefore performed. Histological examination revealed bland spindle-cell proliferation arranged in fascicles, with mitotic activity of < 1 per 10 high-power fields and a Ki-67 labeling index of approximately 2%. The spindle cells expressed desmin, vimentin, and estrogen receptor, whereas focal TTF-1 staining was restricted to entrapped bronchial epithelial cells. In conjunction with the bilateral multifocal pulmonary distribution and remote history of uterine leiomyoma, these findings supported a clinicopathological diagnosis of pulmonary BML. The patient recovered uneventfully without endocrine therapy. During postoperative telephone follow-up, she reported no new discomfort, and regular chest CT surveillance was recommended. Conclusion Pulmonary BML should be considered in the differential diagnosis of multiple pulmonary nodules in women with a remote history of uterine leiomyoma. Mild FDG uptake cannot distinguish pulmonary BML from a low-grade malignancy. Integrated clinical, radiological, and pathological assessment is therefore required to establish the diagnosis and avoid unnecessary treatment.
BackgroundLow-grade fibromyxoid sarcoma (LGFMS) is an uncommon malignant fibroblastic neoplasm characterized by deceptively bland histology and risk of late recurrence and metastasis. Primary pulmonary LGFMS is rare, with fewer than a dozen reported patients. Because the lung is also the most frequent metastatic site f...
Nathan Do, Daffolyn Rachael Fels Elliott, Anders Meyer et al.· International Journal of Sur...· 0 citations
A 52-year-old female patient was initially evaluated at another hospital for a splenic tumor. Chest computed tomography revealed a 12-mm nodule with well-defined margins and uniform internal density in the S5 segment of the right middle lobe. She was referred to our hospital for follow-up of a suspected benign lung tum...
Yuuya Tomioka, H. Kubokura, Mana Okuni et al.· Journal of Nippon Medical Sc...· 0 citations
Background: Pulmonary carcinoid tumors are rare, well-differentiated neuroendocrine neoplasms accounting for approximately 1–2% of all primary lung malignancies. Although pulmonary carcinoids generally exhibit an indolent clinical course, atypical carcinoids may show more aggressive behavior with an increased risk of l...
Latifa Doublali, Adnane Adnani, Houda Bentayaa et al.· European Journal of Medical...· 0 citations
Primary leiomyosarcoma of the ovary is extremely rare, accounting for only 1% of ovarian tumors. Myxoid leiomyosarcoma (MLMS) is one of the subtypes. As far as we know, only few cases have been reported, and there is no imaging report of ovarian MLMS. This paper reports a case of primary MLMS of the ovary with multiple...
Ling Wang, Peng Sun, Kun Jiang et al.· Asia Oceania Journal of Nucl...· 0 citations
BACKGROUND Hepatic epithelioid hemangioendothelioma (HEHE) is a rare vascular tumor of endothelial origin with variable clinical behavior, posing significant diagnostic and therapeutic challenges. Due to its nonspecific presentation and diverse imaging features, it is frequently misdiagnosed. We present a unique case o...
Zhe Tang, Fan Gao, Jie Lian et al.· The American journal of case...· 0 citations
Inflammatory myofibroblastic tumor (IMT) is a rare mesenchymal neoplasm of intermediate malignant potential, most commonly arising in the lung. Although generally indolent, distant metastases occur in a minority of cases and can generate major diagnostic uncertainty, particularly when the central nervous system is invo...
Alaoui Y. Mhamdi, A. A., Ouazzani H. et al.· World Journal of Advanced Re...· 0 citations
We use cookies to run the site and, with your consent, for analytics and to show ads.
See our Cookie Policy.