Hoo P S, Norhaslinda A R, Reza J N Shah
Obstetrics & Gynaecology Department, School of Medical Science, Universiti Sains Malaysia, Kubang Kerian, Kelantan, Malaysia.
Case Rep Obstet Gynecol. 2016;2016:3725043. doi: 10.1155/2016/3725043. Epub 2016 Oct 23.
We report a case of adenomyosis which developed from a hypoplastic uterus and leiomyoma in a patient with MRKH syndrome. A 45-year-old Malay female with primary amenorrhoea and primary infertility presented with abdominal mass and abdominal pain. She is phenotypically female, has well developed secondary sexual characteristics, and has normal female external genitalia with shallow vagina dimple. Transabdominal ultrasonography showed a homogenous adnexal mass of 10 × 8 cm, uterus sized 5 × 4 cm, and normal kidneys. A complex mass of right adnexa was demonstrated by CT scan. Exploratory laparotomy showed torsion of right adnexal mass and rudimentary uterus with fibroid but no endometrial tissue and blind end with absent cervix. The normal right ovary and tube were not visualized. The left fallopian tube and ovary were normal. It is also complicated by vaginal agenesis. Removal of right adnexal mass and rudimentary uterus was done with preservation of left ovary. The histologic diagnosis was uterine adenomyosis and leiomyoma arising from the right adnexa, possibly from the broad ligament.
我们报告了一例苗勒管发育不全综合征患者,其发育不全的子宫和平滑肌瘤发生了子宫腺肌病。一名45岁的马来女性,原发性闭经且原发性不孕,出现腹部肿块和腹痛。她表型为女性,第二性征发育良好,女性外生殖器正常,阴道有浅凹痕。经腹超声检查显示附件区有一个10×8 cm的均匀肿块,子宫大小为5×4 cm,肾脏正常。CT扫描显示右侧附件区有一个复杂肿块。剖腹探查显示右侧附件肿块扭转,子宫发育不全伴有肌瘤,但无子宫内膜组织,宫颈缺失呈盲端。未见到正常的右侧卵巢和输卵管。左侧输卵管和卵巢正常。该病例还合并阴道发育不全。在保留左侧卵巢的情况下,切除了右侧附件肿块和发育不全的子宫。组织学诊断为子宫腺肌病和平滑肌瘤,起源于右侧附件,可能来自阔韧带。