LAUSR

Sir, Sex cord tumor with annular tubules (SCTAT), first described by Scully RE, is a rare ovarian tumor which accounts for only 1.4% of all sex cord stromal tumors of the ovary. About one-third of cases of SCTAT are associated with Peutz-Jeghers syndrome (PJS). The syndromic tumors are more likely to be bilateral and small and behave in a benign fashion. The non-syndromic tumors are large and unilateral and more likely to behave aggressively [1]. A 26-year-old unmarried lady presented to the Gynecology Outpatient Department with complaints of polymenorrhea, pain, and distension of abdomen. On per abdomen examination, a 16-week-size mass was palpable. The mass was firm and non-tender. Subsequent ultrasound abdomen showed an echogenic lesion with internal cystic areas in left adnexa. Contrast enhanced computed tomography (CECT) abdomen showed a heterogeneously enhancing predominantly solid lesion in left adnexa measuring 8.5 × 16.1 × 11.4 cm. The uterus and cervix were normal. Tumor markers CA125, serum LDH, serum alpha fetoprotein (AFP), and carcinoembryonic antigen (CEA) were within normal limits. Serum inhibin levels were elevated at 209 pg/ml. Exploratory laparotomy with left salpingo-oophorectomy was done. Omental and peritoneal biopsies were taken. Grossly, the ovarian tumor mass was solid and cystic with large areas of hemorrhage. On mic roscopy, the tumor was composed of circumscribed ring–shaped tubules with peripherally oriented nuclei with central hyalinized basement membrane– like material. Both simple and complex tubules were noted. The nuclei had vesicular chromatin and grooves. No germ cell component was seen [Fig. 1a–d]. On immunohistochemistry, the tumor cells were immunopositive for inhibin, calretinin, CD99, CD10, and vimentin and negative for pan cytokeratin. The Ki 67 index was 14% [Fig. 2a–f]. The patient did not show features of Peutz-Jegher’s syndrome. Final diagnosis was non-syndromic sex cord stromal tumor with annular tubules with peritoneal tumor deposit. Two months after the surgery, the patient developed tumor recurrence with a 2 × 1-cm solid enhancing lesion in left adnexa and mesenteric deposits. A complete recurrent tumor resection was performed at some other center and the patient was tumor-free at 2 months follow-up. A complete tumor resection has been the mainstay of treatment for recurrent and malignant cases. However, recently, taxane plus bevacizumab has been tried in cases not amenable to complete resection [2]. Almost all the SCTATs arise from the ovary with only rare extraovarian a nd t e s t i c u l a r t umo r s b e e n r e po r t e d [ 3 , 4 ] . Histogenetically, these tumors have features intermediate between granulosa cell tumors and Sertoli cell tumors. Adenoma malignum of the cervix is also associated with Peutz-Jeghers syndrome and sometimes occurs in conjunction with SCTAT [5]. To conclude, SCTAT should be included in the differential diagnosis of sex cord stromal tumors even in the absence of features of PJ syndrome given the higher potential for aggressive behavior in such cases. * Nadeem Tanveer [email protected]