Zamir Naima
Dr. Naima Zamir, Associate Professor, National Institute of Child Health, Karachi, Pakistan.
Pak J Med Sci. 2020 Jan-Feb;36(2):187-191. doi: 10.12669/pjms.36.2.1095.
To document our experience of initial management of Cloacal malformation in female patients.
A descriptive retrospective study was conducted in the Department of Pediatric Surgery of the National Institute of Child Health Karachi from January 2010 to September 2018. Female patients with diagnosis of Cloacal malformation were included in this study. Data regarding the age at presentation, mode of presentation, clinical features, presence of hydrocolpos, and associated anomalies were noted. Surgical procedures performed in these patients and the outcomes were also documented. Data was analyzed on SPSS Version 20.
Sixty females were included in the study. Age ranged from birth to three years with a median of four days. Patients admitted through emergency were 44 (73.33%) while 16 (26.66%) were admitted through outpatient clinic. Hydrocolpos was found in 15 (25.00%) patients. Five (8.33%) patients had massive abdominal distention and were presented with severe respiratory distress. Among them three had massive hydrocolpos, one patient had pneumoperitoneum secondary to Meckel's perforation and one patient was having massive colonic dilatation. Hydronephrosis and hydroureter were found in 14 (23.33%) patients, while dilated bladder was found in three (5.00%) patients. After optimization of patients, bowel diversion was done as transverse colostomy in 39 (65.00%) patients, high sigmoid colostomy in 17(28.33%) patients while ileostomy was done in three (5.00%) patients. All patients with hydrocolpos had tube vaginostomy. None of the patients required bladder diversion and urinary tract dilatations were gradually subsided in nine patients in the post-operative period. Associated anomalies were found in 22(36.66%) of cases predominantly of sacral origin. Operative complications were found in 18(30.00%) patients, including stoma site in infection in 12(20.00%) patients, vaginal tube dislodgement in two patients, wrong placement of tube in one patient and vaginostomy stenosis in one case. While bowel stoma retraction occurred in four patients, prolapsed was found in three patients. Renal failure occurred in one patient. In total, 37(61.00%) patients had smooth recovery, 18(30.00%) patients had some complications, while Five (8.33%) patients were expired due to sepsis.
Majority of cloacal malformations present in neonatal life. Initial management is an important step in dealing with these patients. Care must be taken during the abdominal exploration regarding drainage of hydrocolpos and appropriate placement of bowel stoma.
记录我们对女性泄殖腔畸形初始治疗的经验。
2010年1月至2018年9月在卡拉奇国家儿童健康研究所小儿外科进行了一项描述性回顾性研究。本研究纳入诊断为泄殖腔畸形的女性患者。记录患者的就诊年龄、就诊方式、临床特征、处女膜膨出的存在情况以及相关异常。还记录了这些患者所进行的外科手术及结果。数据在SPSS 20版本上进行分析。
本研究纳入60名女性。年龄范围从出生至3岁,中位数为4天。通过急诊入院的患者有44名(73.33%),而通过门诊入院的有16名(26.66%)。15名(25.00%)患者发现有处女膜膨出。5名(8.33%)患者有严重腹胀并伴有严重呼吸窘迫。其中3名有巨大处女膜膨出,1名患者因梅克尔憩室穿孔导致气腹,1名患者有巨大结肠扩张。14名(23.33%)患者发现有肾盂积水和输尿管积水,而3名(5.00%)患者发现膀胱扩张。在对患者进行优化处理后,39名(65.00%)患者行横结肠造口术进行肠道转流,17名(28.33%)患者行高位乙状结肠造口术,3名(5.00%)患者行回肠造口术。所有有处女膜膨出的患者均行了阴道造瘘术。没有患者需要膀胱转流,9名患者在术后尿路扩张逐渐消退。22例(36.66%)病例发现有相关异常,主要起源于骶骨。18名(30.00%)患者出现手术并发症,包括12名(20.00%)患者造口部位感染,2名患者阴道造瘘管移位,1名患者造瘘管放置错误,1例阴道造瘘狭窄。4名患者出现肠造口回缩,3名患者出现脱垂。1名患者发生肾衰竭。总体而言,37名(61.00%)患者恢复顺利,18名(30.00%)患者有一些并发症,5名(8.33%)患者因败血症死亡。
大多数泄殖腔畸形在新生儿期出现。初始治疗是处理这些患者的重要一步。在腹部探查过程中必须注意处女膜膨出的引流和肠造口的恰当放置。