A Rare Congenital Anomaly of the Urogenital System

1959 ◽  
Vol 147 (3) ◽  
pp. 164-171
Author(s):  
K.J.H. Verschoof
Keyword(s):  
Congenital Anomaly ◽  
Urogenital System ◽  
Rare Congenital Anomaly

scholarly journals Congenital Agenesis of the Left Lung: A Rare Case

2011 ◽  
Vol 1 ◽  
pp. 47 ◽  
Author(s):  
Tülin Durgun Yetim ◽  
Hanifi Bayaroğullari ◽  
Hülya Polat Yalçin ◽  
Vefik Arιca ◽  
Seçil Gunher Arιca
Keyword(s):  
Congenital Anomaly ◽  
Rare Case ◽  
Left Lung ◽  
Urogenital System ◽  
Pulmonary Agenesis ◽  
Rare Congenital Anomaly ◽  
Congenital Agenesis

Pulmonary agenesis is a rare congenital anomaly, the etiology of which is not clearly known. Other systemic comorbidities such as cardiovascular, gastrointestinal, musculoskeletal, and urogenital system anomalies can be observed in more than half of the patients. It is usually diagnosed during childhood. Diagnosis in adulthood is very rare. We present a case of pulmonary agenesis diagnosed in an adult.

scholarly journals TRIORCHIDISM WITH TORSION OF ACCESSORY TESTIS: A CASE REPORT

2020 ◽  
Vol 4 (6) ◽  
Author(s):  
Vishal Prashar ◽  
Shamsher Singh
Keyword(s):  
Congenital Anomaly ◽  
Case Report ◽  
Inguinal Hernia ◽  
Ct Scan ◽  
Urogenital System ◽  
Sudden Increase ◽  
Rare Congenital Anomaly ◽  
History Of

Polyorchidism is an extremely rare congenital anomaly of the urogenital system and is defined as the presence of more than two testes. The majorities of patients are asymptomatic or present with painless inguinal or scrotal masses. We present the case of an 31-year-old male presented in surgery opd with pain and sudden increase in size of swelling right groin. Although it was present since birth but it was painless and small in size.  No history of trauma, fever, pus discharge.  On examination single ovoid mobile tender swelling was present in right groin, overlying skin was normal and bilateral testis and penis was normal. USG and CT scan showed triorchidism with torsion of accessory testis. Exploration was done under LA and accessory testis was removed. Polyorchidism is a rare congenital anomaly. Patients with polyorchidism can be managed conservatively unless there are no accompanying problems such as inguinal hernia, cryptorchidism or torsion. Keywords: polyorchidism, Acessory  testis, Triorchidism.

scholarly journals Diphallia, a rare congenital anomaly- A case and literature review

2021 ◽  
Vol 7 (2) ◽  
pp. 51-53
Author(s):  
L Muhindo ◽  
◽  
AA Hadonou ◽  
IK Gandaho ◽  
Toré Sanni R ◽  
...  
Keyword(s):  
Congenital Anomaly ◽  
Literature Review ◽  
General Surgery ◽  
Rare Case ◽  
Urogenital System ◽  
Partial Duplication ◽  
Rare Congenital Anomaly ◽  
Centre Hospitalier ◽  
Centre Hospitalier Universitaire ◽  
Surgery Department

Diphallia or also called diphallus is a malformation of the male urogenital system characterized by a complete or partial duplication of the penis. The authors report one rare case of a newborn baby transferred from pediatrics for better management of a polymalformative syndrome associating diphallia and anal imperforation are treating in Urology unit at general surgery department, Centre hospitalier universitaire departemental Borgou-Alibori, at Parakou City

scholarly journals Cor triatriatum dexter, a very rare congenital anomaly presented in a complex pathological context – case presentation

2014 ◽  
Vol 60 (4) ◽  
pp. 160-162
Author(s):  
Liliana Gozar ◽  
Cristina Blesneac ◽  
Rodica Toganel
Keyword(s):  
Congenital Anomaly ◽  
Cytomegalovirus Infection ◽  
Cor Triatriatum ◽  
Anatomical Feature ◽  
Renal Anomalies ◽  
Anatomical Variant ◽  
Case Presentation ◽  
Congenital Cytomegalovirus ◽  
Rare Congenital Anomaly ◽  
Cor Triatriatum Dexter

Abstract Background Cor triatriatum dexter is an extremely rare congenital anomaly, and in most cases, without hemodynamic significance. Congenital cytomegalovirus infection is the most common viral infection, the majority of infected infants being asymptomatic and only 5-15% being symptomatic in the neonatal period. Case report We present the case of a female infant, aged 3 months. Clinical examination reveals cranial and facial anomalies. The karyotype was normal. Laboratory tests revealed the presence of anti-CMV antibodies in urine. Imaging studies showed cerebral and renal anomalies. Echocardiographic exam revealed a congenital anatomical feature without hemodynamic significance - cor triatriatum dexter. Conclusions although cytomegalovirus infection is mostly asymptomatic, it can present as a complex pathological association, in which a congenital cardiac anatomical feature without hemodynamic significance, considered by some authors as an anatomical variant, can appear

scholarly journals Roberts uterus: a rare congenital anomaly

2017 ◽  
Vol 6 (12) ◽  
pp. 5657
Author(s):  
Nagendra Sardeshpande ◽  
Pratima Chipalkatti ◽  
Jainesh Doctor
Keyword(s):  
Congenital Anomaly ◽  
Abdominal Pain ◽  
Adnexal Mass ◽  
Lower Abdominal Pain ◽  
Uterine Horn ◽  
Transabdominal Ultrasound ◽  
Septate Uterus ◽  
Bicornuate Uterus ◽  
Rare Congenital Anomaly ◽  
Hysteroscopic Resection

A 23-year-old girl presented with severe cyclical lower abdominal pain during menstruation since menarche, which had increased since the last 4 years. Transabdominal ultrasound showed adnexal mass with no internal vascularity; MRI reported it as bicornuate uterus with one non-communicating right uterine horn with haematometra. On hysteroscopy there was evidence of septate uterus communicating only to the left ostia. Ultrasonography-guided hysteroscopic resection of septa with drainage of haematometra was done. Patient is presently asymptomatic.

CONGENITAL METACARPAL SYNOSTOSIS TREATED BY DOUBLE BONE BLOCKS TECHNIQUE: A CASE REPORT FROM THAILAND

Hand Surgery ◽  
2005 ◽  
Vol 10 (01) ◽  
pp. 131-134 ◽  
Author(s):  
Surut Jianmongkol ◽  
Tala Thammaroj ◽  
Kitiwan Vipulakorn
Keyword(s):  
Congenital Anomaly ◽  
Case Report ◽  
Surgical Techniques ◽  
Rare Condition ◽  
Rare Congenital Anomaly

Congenital metacarpal synostosis is a rare congenital anomaly in the hand, especially in our area. There were several reports of surgical techniques for correction deformities. We report this rare condition in our hospital and treatment with the metacarpal osteotomy and double bone blocks technique of grafting.

Splenogonadal Fusion: A Rare Congenital Anomaly in Children

BJUI ◽  
2012 ◽  
Author(s):  
Osman Zeki Karakus ◽  
Mustafa Ozcetin ◽  
Fikret Erdemir
Keyword(s):  
Congenital Anomaly ◽  
Splenogonadal Fusion ◽  
Rare Congenital Anomaly
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