Surgical therapy for herlyn-werner-wunderlich (HWW) syndrome cases

Pangastuti N, Rahman Mn, Setyawan N
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Abstract

Introduction: One of the rare forms of Mullerian congenital ducts is Herlyn-Werner-Wunderlich (HWW) syndrome. HWW syndrome is usually found at puberty with nonspecific symptoms. Pelvic pain can be found both acute and chronic, dysmenorrhoea, as well as hematometra and hematocolpos. Early detection and treatment results in a good prognosis with fertility preservation. Case presentation: Two cases of Herlyn-Werner-Wunderlich (HWW) syndrome surgically performed were reported at Dr. Sardjito Yogyakarta Indonesia Central General Hospital in 2017-2018. Both cases are still children and at the age of puberty. The chief complaint in both cases it was reported to have the same main complaint, abdominal pain, with the condition having never experienced menstruation yet. On further examination it is known that pain is caused due to hematometra and hematosalping that occur in both cases. The first case with hematometra in the right hemiuterus and right hematosalpinx, while second case with hematometra in the uterus didelphys and bilateral hematosalpinx. One case with a normal vagina, and the other case of vaginal agenesis. There was previous history of surgery in both of cases. There are abnormalities in the urinary tract that occur together with these genital abnormalities. Surgical therapy is carried out with the main goal being to drain menstrual blood from hematometra and hematosalpinx. In first case which has a vagina within the normal range (9 cm long) and the inferior area of ​​the right hemiuterus which is bulging toward the vagina, an area can be identified for the drainage incision to drain the entire hematometra and hematosalpinx. In the second case with vaginal agenesis, neovagina which is made by sigmoid colon vaginoplasty surgery can be a way of menstrual blood flow for a lifetime. Conclusion: Clinical manifestations of Herlyn-Werner-Wunderlich (HWW) syndrome cases can be classified into 2 groups, complete and incomplete. Surgical treatment is based on the condition of the uterus and vagina. In the condition of cervical agenesis but with a normal vagina, surgery can be done by making an incision in the drainage of the uterine cervical tissue. If vaginal agenesis is obtained, vaginoplasty surgery can be performed, and one of the options is sigmoid colon vaginoplasty.
herlin -werner-wunderlich综合征的手术治疗
简介:一种罕见形式的先天性苗勒氏管是herlin - werner - wunderlich (HWW)综合征。HWW综合征通常在青春期发现,无特异性症状。盆腔疼痛可发现急性和慢性,痛经,以及积血和积血。早期发现和治疗结果预后良好,生育能力保存。病例介绍:2017-2018年在Dr. Sardjito印度尼西亚日惹中央总医院报告了2例手术治疗的herlin - werner - wunderlich (HWW)综合征。这两个病例都是儿童,处于青春期。据报道,这两个病例的主诉都有相同的主诉,腹痛,而且从未经历过月经。进一步检查可知,疼痛是由于两种情况下发生的积血和出血引起的。1例为右半子宫及右侧输卵管积血,2例为子宫积血及双侧输卵管积血。1例阴道正常,1例阴道发育不全。两例患者均有手术史。泌尿道的异常与这些生殖器异常一起发生。手术治疗的主要目的是将经血从血肿和输卵管排出。在第一种情况下,阴道在正常范围内(9厘米长),右半子宫下半区向阴道膨出,可以确定一个区域用于引流切口,以排出整个积血和输卵管积血。在阴道发育不全的第二种情况下,通过乙状结肠阴道成形术制造的新阴道可以成为一生的经血流动方式。结论:HWW综合征的临床表现可分为完全型和不完全型两组。手术治疗是基于子宫和阴道的状况。在宫颈发育不全但阴道正常的情况下,可以通过在宫颈组织的引流处做一个切口来进行手术。如果阴道发育不全,可以进行阴道成形术,其中一种选择是乙状结肠阴道成形术。
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