Pulmonary benign metastasizing leiomyoma: a case report and review of the literature
© Fu et al.; licensee BioMed Central Ltd. 2012
Received: 13 April 2012
Accepted: 26 November 2012
Published: 12 December 2012
Pulmonary benign metastasizing leiomyoma characterized by the growth of uterine leiomyoma in the lung is a very rare disease. We herein report the case of a 46-year-old asymptomatic woman who underwent a total abdominal hysterectomy for her multiple uterine leiomyomas 5 years ago, with the presence of multiple shadows in her chest roentgenogram during the regular check-up. Chest computerized tomography (CT) showed multiple solitary nodules in both lungs. Video-assisted thoracoscopic surgery with a wedge resection of the lesion was performed. Histopathologically, the pulmonary nodule was composed of benign smooth muscle cells and demonstrated low mitotic activity and absence of necrosis. Immunohistochemical staining for smooth muscle actin (SMA) and Desmin were extremely positive. CD10, CD117 and S-100 were negative in the tumor cells. Positive immunoreactivity for estrogen receptor (ER) and progesterone receptor (PR) were detected. The pathological diagnosis was pulmonary benign metastasizing leiomyoma.
KeywordsLung Leiomyoma Benign lesion Metastases
Pulmonary benign metastasizing leiomyoma is a very rare disease characterized by the growth of uterine leiomyoma tissue in the lung . In most cases, there is a previous history of total abdominal hysterectomy for uterine leiomyoma. However, the pathogenesis of this disease has not yet been elucidated.
The patient was discharged from the hospital without any early postoperative complications. She started taking mifepristone (12.5 mg daily) and receiving Zoladex injections (3.6 mg every 4 weeks). Her current general condition was satisfactory without any radiological evidence of recurrent disease or distant metastases. The remaining lesions in both lungs were stable during the follow-up period.
Benign metastasizing leiomyoma is a very rare disease in which tissue from a benign uterine leiomyoma is detected as a solitary nodule or as multiple nodules in the lungs of patients with a previous history of hysterectomy for uterine leiomyoma. In 1939, Steiner et al. reported the first case in which a leiomyoma transferred from the uterus to the lung, showing a benign histological appearance. It was called “metastasizing fibroleiomyoma” . Since then there have been several similar reports, and it was renamed benign metastasizing leiomyoma.
Most patients with benign metastasizing leiomyoma are asymptomatic. It is usually found during physical examinations. Abramson et al. reported that the average age of patients with benign metastasizing leiomyoma is 48 years old, with the period from hysterectomy to nodule detection varying from 3 months to 26 years . Horstmann et al. reported that the radiological presentation of pulmonary benign metastasizing leiomyoma is as multiple nodules in 87% of cases (70% bilateral nodules and 17% unilateral nodules) or as a solitary nodule in 13% of cases . The main metastatic site of benign metastasizing leiomyoma is the lung, but other sites including the lymph nodes, soft tissue of the pelvis, bone, bone marrow, greater omentum, peritoneum and heart have also been reported . Tsunoda et al. reported the first case of benign metastasizing leiomyoma of the lung complicated with primary lung cancer .
The nature and etiology of benign metastasizing leiomyoma are still controversial. Uterine leiomyoma has been reported to depend on hormones [1, 6]. Estrogen receptor and progesterone receptor in case of benign metastasizing leiomyoma usually have high expression, and drugs or ovariectomy can make the lesions regress or remain stabilized. This provides us with a basis for believing that estrogen and progesterone may play an important role in the course of pathogenesis. However, Patton et al. have previously reported that benign metastasizing leiomyoma results from the monoclonal, hematogenous spread of an apparently benign uterine leiomyoma, most likely leading to secondary intravenous leiomyomatosis .
Making the diagnosis of benign metastasizing leiomyoma is very difficult, and it has strict pathological diagnostic criteria. It is based on the results of the immunohistochemical staining and the history of hysterectomy for uterine leiomyoma. In our case the pathological examination showed spindle-shaped cells without mitotic activity or nuclear atypia. The tumor cells are strongly positive for SMA, confirming the smooth muscle origin of this benign tumor. In addition to these features, immunohistochemical staining is negative for CD117, ruling out an extra-gastrointestinal stromal tumor, and all of the cells are negative for S100, essentially excluding a tumor of neural origin. Positive immunoreactivity for estrogen receptor (ER) and progesterone receptor (PR) suggests the spindle-shaped cells are uterine smooth muscle cells.
Review of the current literature
Refused hormone therapy after surgery
Treatment with leuprolide acetate
Monthly injections of depot GnRH analogs
Taking an aromatase inhibitor (Letrozole® 2.5 mg daily, Femara)
Patient 1.Taking the long-acting GnRH agonist, leuprolide acetate. Five months later, an AI at a dose of 1 mg daily was added. Refused the addition of an LHRH agonist
Patient 2. On follow-up a month after discharge, the patient was convinced to restart raloxifene 120 mg daily and anastrozole 2 mg daily
Treatment with cytostatic in 2 patients, with hormonal therapy in 2 and observation in 6
Although BML is a very rare condition, it should be considered in asymptomatic women of reproductive age with a history of uterine leiomyoma who present with solitary or multiple pulmonary nodules of the lung. Long-term close surveillance is required for patients with BML for early detection of recurrence or distant metastases.
Written consent was obtained from the patient for the study and publication of this case report and accompanying images. A copy of written consent is available for review from the Editor-in-Chief.
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