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- DOI 10.18231/j.ijmpo.2020.042
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- Citation
A case report of large hydrometrocolpos in neonate
- Author Details:
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Nilesh T Shah *
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Mohammad Gandhi
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Parul Valia
Introduction
Hydrometrocolpos is an accumulation of uterine and vaginal secretions as well as menstrual blood in the uterus and vagina. Usually this condition manifests at puberty caused by an obstruction of the female genital tract. The most frequent cause of hydrometrocolpos is the presence of imperforate hymen due to failure of partial resorption of this membrane during the embryonic development, the incidence is 0.0014-0.1% in full-term newborns.[1], [2] Congenital hydrometrocolpos is a rare event with an incidence of about 0.006%.[3] Incidence of McKusick-Kaufman syndrome. is 1:10,000.
Description
2hrs old female delivered at 38 weeks of gestation, birth weight 2.8kg with abdominal distension with all four limb Polydactyly, vulval odema and lower limb odema. Prenatal US examinations showed lower abdominal cystic mass with mild hydroureter and mild hydronephrosis ([Figure 1]).
US examination was showed an inhomogeneous hypoechoic and corpusculated cystic formation of about 12*6cm with well demarcated margins; located in mid region of the abdomen extending from the upper middle to the lowest region. The bladder was empty and compressed. B/L mild hydroureter and hydronephrosis, uterus was not visible.
Hydrometrocolpos was suspected and subsequently confirmed by physical examination of the external genitalia, showed vulval edema along with lower limb edema. Vaginoscopy guided hysteroscopy carried out and hysteroscopic drainage of approx. 100ml hydrometra. Subsequent US imaging showed normal appearance of the uterus and vagina.

Discussion
Huge abdominal swelling is a relatively uncommon presentation for newborn babies. The common differential diagnoses to be considered in such babies include neuroblastoma, intra-peritoneal fluid collection following organ failure, ovarian cysts, intra-abdominal sacrococcygeal teratoma, mesoblastic nephroma, bowel duplication, genitourinary anomalies and anterior sacral meningocele.[4]
Hydrometrocolpos occurs by genital tract obstruction is associated with accumulation of cervical and endometrial gland secretions.
This condition caused by congenital malformations of the genital tract such as vaginal atresia, transverse vaginal septum and imperforate hymen. It may be associated with the MKKS, an autosomal recessive disorder characterized by vaginal atresia with hydrometrocolpos, polydactyly, congenital heart defects and nonimmune hydropsfetalis.[5] In our case features of the McKusick-Kaufman syndrome. like hydrometrocolpos, polydactyly, lower limb edema, vulval edema & abdominal wall edema. 2D Echo was normal.
The previously reported low incidence of hydrometrocolpos could be due to difficulty in diagnosis and high mortality rates as suggested by Mittal et al. [6]
MKKS is a very rare disorder. Incidence is 1:10,000. Caused by mutation of gene which play Important role in protein called “chaperonin” which is important for formation of the limbs, heart and reproductive system.
As described in other cases,[7] hydrometrocolpos is usually diagnosed prenatally as the cause of abdominal cystic mass. However, in the present case prenatal examinations were all negative.
Imperforate hymen is a result of the hymen failing to rupture during the eighth week of gestation.
In hydrometrocolpos caused by imperforate hymen, hymenectomy has proved to be an adequate, conservative treatment.[8]
Differential diagnosis of abdominal mass are ovarian cysts, intraabdominal sacrococcygeal teratoma, neuroblastoma mesoblastic nephroma, bowel duplication, gross hydronephrosis, renal cyst, urachal cyst, hydrometrocolpos, choledocal cyst.
Hydrometrocolpos cause urinary stasis and acute renal failure due to obstructive uropathy.[9], [10] In this case, physical and US examinations showed a large hypoechoic mass in the mid region of the abdomen extending from the upper middle to the lowest region and B/L mild hydroureter and mild hydronephrosis.
Hydrometrocolpos is a possible cause of huge abdominal swelling in a newborn. Imperforate hymen and obstructive uropathy could be associated conditions. Clinicians should consider the possibility of hydrometrocolpos as a cause of huge abdominal swelling in newborns. The genitals should be carefully examined to save patients from major surgeries and related complications
In conclusion, although hydrometrocolpos is a rare event, should be kept in mind if pre and/or postnatal examinations reveal the presence of pelvic mass.
Conflicts of Interest
All contributing authors declare no conflicts of interest.
Source of Funding
None.
References
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How to Cite This Article
Vancouver
Shah NT, Gandhi M, Valia P. A case report of large hydrometrocolpos in neonate [Internet]. IP Int J Med Paediatr Oncol. 2025 [cited 2025 Sep 05];6(4):178-180. Available from: https://doi.org/10.18231/j.ijmpo.2020.042
APA
Shah, N. T., Gandhi, M., Valia, P. (2025). A case report of large hydrometrocolpos in neonate. IP Int J Med Paediatr Oncol, 6(4), 178-180. https://doi.org/10.18231/j.ijmpo.2020.042
MLA
Shah, Nilesh T, Gandhi, Mohammad, Valia, Parul. "A case report of large hydrometrocolpos in neonate." IP Int J Med Paediatr Oncol, vol. 6, no. 4, 2025, pp. 178-180. https://doi.org/10.18231/j.ijmpo.2020.042
Chicago
Shah, N. T., Gandhi, M., Valia, P.. "A case report of large hydrometrocolpos in neonate." IP Int J Med Paediatr Oncol 6, no. 4 (2025): 178-180. https://doi.org/10.18231/j.ijmpo.2020.042