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Adenomyosis in a noncommunicating rudimentary horn of unicornuate uterus - a diagnostic dilemma

机译:独角兽子宫不交流的角状腺中的腺肌病-诊断困境

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The prevalence of congenital uterine malformations is about 0.5%.Unicornuate uterus is a rare anomaly of the female internal genitalia (2.5-13%) [1]. Partial development of one of the mullerian ducts may result in anomalies in various combinations whereby one of the horns may remain rudimentary with or without any communication with its fellow [1]. Complications related to this condition are related to its presentation during different phases of life of a woman. We present a case of adenomyosis in the noncommunicating laterally displaced rudimentary horn which gave us a primary impression of solid ovarian tumor. Case Report A 45 year old woman, Para 2, presented with a lump in her lower abdomen which had increased in size since past 18 months. She had regular menstrual cycles but felt pain in the lower abdomen as well as in the low back region during menses. There was no significant loss of weight or alteration of bladder or bowel habits. She had borne three children vaginally. In her first pregnancy she had pregnancy induced hypertension and delivered breech vaginally. Her second pregnancy was uneventful but she had an intrauterine fetal death (IUFD) at term in her third pregnancy. She is a short statured woman (4ft 9 in) and clinical examination revealed a large and firm smooth surfaced, non-tender lump of about 16 weeks gravid uterine size arising from the pelvis without any restriction in mobility. The lower pole could be delineated with ease. There was no evidence of free fluid in the peritoneal cavity. Vaginal examination revealed uterus and left adnexa normal, and on the right a firm mobile mass consistent with the abdominal examination. USG of whole abdomen revealed a mass on the right side with normal uterus and left ovary. Right ovary could not be seen and the final impression was either a subserous fibroid or an ovarian tumor. There was no abnormality in renal tract.Laparotomy was performed through Pfanenstiel incision. A mass (about 12 x 15cm.) was seen attached to the horn of the unicornuate uterus on left side. Round ligament, tube and ovary was attached to the left side. Right ovary and tube was seen separately connected to the solid mass but the round ligament on this side was obscured probably due to stretch. Both tubes and ovaries looked healthy. Total abdominal hysterectomy with bilateral salpingo-oophorectomy was performed. The specimen was thoroughly studied postoperatively [Fig 1, Fig 2] and cut open to identify the cavity in both the mass and the uterus. The cut surface of the mass showed scattered areas of tiny hemorrhagic spots [Fig 3].
机译:先天性子宫畸形的患病率约为0.5%。单角子宫是女性内部生殖器的罕见异常(2.5-13%)[1]。富勒管之一的部分发展可能导致各种组合的异常,从而使其中一个角可能保持基本状态,无论是否与它的同伴沟通[1]。与这种状况有关的并发症与妇女生命不同阶段的表现有关。我们在非交流的横向移位的基本角中呈现出子宫腺肌病的情况,这给了我们对卵巢实性肿瘤的初步印象。病例报告一名45岁的女性,第2段,下腹部有一个肿块,该肿块自过去18个月以来一直在增大。她的月经周期规律,但在月经期间,小腹和腰部区域感到疼痛。没有明显的体重减轻或膀胱或肠道习惯改变。她已经生了三个孩子阴道。在她的第一次妊娠中,她患有妊娠高血压病,并且阴道分娩臀位。她的第二次怀孕很顺利,但是第三次​​怀孕足月胎儿宫内死亡(IUFD)。她是个矮矮胖胖的女人(4英尺9英寸),临床检查显示,骨盆引起的子宫大小大而结实,表面光滑,没有嫩滑的肿块,约16周,没有任何活动受限。下极可以轻松划定。没有证据表明腹膜腔内有游离液体。阴道检查显示子宫和左附件正常,而右侧则有牢固的活动性肿块,与腹部检查一致。整个腹部的USG显示右侧肿块,子宫正常,左卵巢。右卵巢未见,最终印象是浆膜下肌瘤或卵巢肿瘤。肾脏未见异常,通过Pfanenstiel切口进行剖腹手术。看到一块肿物(约12 x 15厘米)附着在左侧单角子宫的角上。圆形韧带,管和子房附接到左侧。观察到右卵巢和输卵管分别与实体团相连,但此侧的圆形韧带可能由于拉伸而被遮盖。试管和卵巢都看起来很健康。进行全腹子宫切除术与双侧输卵管卵巢切除术。术后对标本进行了彻底研究[图1,图2],将其切开以识别肿块和子宫腔。肿块的切面显示出散布着微小出血点的区域[图3]。

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