Leiomyoadenomatoid Tumors of the Uterus: A Case Report and Literature Review.

A 35-year-old woman arrived at the Obstetrics and Gynecology clinic with concerns for lower abdominal pain. The pain started 3 months previously, was characterized by intermittent occur-rences, and was usually managed with regular analgesia. No constitutional symptoms were recorded. The patient’s menstrual history was regular; however, 7 months prior to her presentation, her menses became heavy and was associated with severe lower abdominal pain. During the physical examination, the patient appeared conscious, oriented, and alert. Her vital signs were within the standard ranges. The abdominal examination revealed a soft and lax abdomen with no masses or tenderness. Other systemic examinations were unremarkable. The initial investigation, which consisted of a complete blood count, blood electrolytes, and hepatic function tests, were all within the standard ranges. A radiological study was conducted, including an ultrasound, revealing multiple uterine fibroids. Based on the clinical and radiological findings, a myomectomy was performed, and the specimen was sent for histopathology examination. On gross examination, multiple well-circumscribed white-tan pieces were noted, and the largest piece measured 9.0×3.0×2.5 cm. The others measured in aggregate 3.0×2.0×0.5 cm. The outer surfaces of all pieces were smooth and characterized by trabeculae, white-tan firm surfaces, and a whorled appearance. As shown in Figure 1 , no necrosis or hemorrhage was seen. The microscopic testing uncovered bundles of smooth muscle arranged in fascicles separated by well-vascularized connective tissue. The cells were elongated with eosinophilic cytoplasm and distinct cell membranes. A gland-like, tubular, and slit-like structure infiltrated the smooth muscle. Those structures were lined by a flattened cuboidal lining with small and uniform nuclei and contained a scanty and eosinophilic cytoplasm, as illustrated in Figure 2A–2D . The mitosis was rarely less than 3 per 10 high-power fields. No necrosis was observed. Immunohistochemistry revealed diffuse strong staining to the calretinin and D2-40, as displayed in Figure 2E–2F ; low-molecular-weight cytokeratin (CK7); wide-spectrum CKs; and a negative reaction to CK20, endothelial antigens (CD31), and Ki 67, which revealed a low proliferative index (<3%). The smooth muscle component expressed positive activity in reaction to smooth muscle actin. A follow-up appointment 3 months afterward showed the patient was doing well, with no signs of recurrence or malignant transformation.

An adenomatoid tumor (AT) is a tumor of mesothelial origin that commonly develops in the male and female genital tracts [ 1 ]. This type of tumor was initially discovered by Sakaguchi in 1916 and was called adenomyomata before Golden et al renamed the condition as “adenomatoid tumor” [ 2 , 3 ]. The microscopic features include the presence of hypertrophied smooth muscle bundled in areas exhibiting anastomosing tubular, gland-like, vascular-like, or cystic branch morphologies. However, when the smooth muscle is exceedingly prominent and gives the appearance of leiomyoma within the AT, the lesion is then referred to as a leiomyoadenomatoid tumor (LMAT) [ 4 ]. Clinically, LMAT is considered an incidental finding during hysterectomies or leiomyoma diagnosis. It is important to recognize these tumors because the prominence of smooth muscle in this particular gland-like structure can mimic features of malignancy. We report the case of a 35-year-old woman with an LMAT incidentally found in her uterus, which was mistaken for a different kind of tumor and was therefore removed as a uterine fibroid. The diagnosis was challenging due to the presence of cribriform gland-like morphology infiltrating the smooth muscle.

An AT is a benign tumor that arises from mesothelial cells [ 4 ]. ATs commonly form in organs covered by mesothelial linings, such as the genital tract, and therefore mainly occur in the testis and uterus [ 4 ]. Extra-genital sites, particularly in the organs closed to serosal membranes (eg, pleura, peritoneum, and pericardium), the adrenal gland, and other visceral organs can be involved [ 5 ]. An AT is usually located subserosally in the posterior wall near the uterine cornu and is < 4 cm in size. Previous studies have mentioned the association between leiomyomata and adenomyosis [ 5 , 6 ]. The microscopic description of the AT shows an intersecting hypertrophied smooth muscle with unremarkable nuclei within a slit-like cystic area as well as glands infiltrating between the muscles lined by round to cuboidal cells. Those cells express immunoreactivity for Wilms tumor-1, calretinin, CK AE1/ AE3, and CK7, as in our case. Differential diagnosis is not uncommon in cases of AT owing to various histological patterns, as mentioned previously. These include leiomyoma, angioleimyoma, leiomyoma with malignancies, malignant mesothelioma, yolk sac tumors, and metastatic adenocarcinoma. AT can mimic leiomyoma or malignant tumors infiltrating smooth muscle when smooth muscle is prominent, thus concealing the AT component. This type of tumor, the LMAT, was described by Epstein in 1992 and is considered a variant of the AT with a prominent smooth muscle component [ 4 ]. In the present case, the first impression was a metastatic tumor infiltrating the smooth muscle, which made it challenging to reach the diagnosis of LMAT. After a review of the available studies published in English on PubMed, Ovid, and Google Scholar, we found only 18 cases that were diagnosed as LMATs, as shown in Table 1 [ 5 – 19 ]. One was in the cervico-uterine junction [ 7 ], 1 was in the ovary [ 8 ], and the remaining 16 cases, in addition to ours, were discovered in the uterus. The patients’ ages ranged from 24 to 76 years, and the size of the tumors ranged from 1.5 to 4 cm. However, the size of the tumor in our case was 9 cm, which was the largest tumor so far, to the best of our knowledge. We found only 1 other case in Saudi Arabia, reported by Junainah et al [ 16 ], and our case is the second reported in the country.

We conducted a literature review on LMATs and reported a case study of a female patient with this condition. An LMAT was found incidentally in the patient’s uterus. We recommend that if the leiomyoma has prominent smooth muscles, LMAT should be considered in the differential diagnosis to avoid being mistaken for an invasive malignancy.