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1.
Autops. Case Rep ; 10(2): e2020155, Apr.-June 2020. graf
Article in English | LILACS | ID: biblio-1131815

ABSTRACT

Diaphragmatic eventration (DE) associated with intestinal malrotation and renal agenesis is a rare entity. The authors report a case of a 69-year-old man who had symptoms of heart failure. He had a previous imaging diagnosis of right diaphragmatic eventration and dilated cardiomyopathy. He died on the second day after the hospital admission and had a post mortem examination that confirmed complete right diaphragmatic eventration, intestinal malrotation, left renal agenesis, dilated cardiomyopathy, and anteriorly rotated right kidney and had findings suggestive of a thoracoabdominal compartment syndrome. Thoracoabdominal compartment syndrome is described as transmission of abdominal pressure through a defective diaphragm causing compression of the hemithorax viscera and mediastinal shift with a hemodynamic alteration. The association of these anomalies is rare, and the possibility of this finding in a patient with eventration should always be considered.


Subject(s)
Humans , Male , Aged , Compartment Syndromes/pathology , Diaphragmatic Eventration/pathology , Kidney/abnormalities , Autopsy , Cardiomyopathy, Dilated , Fatal Outcome
2.
Rev. peru. ginecol. obstet. (En línea) ; 65(2): 213-218, abr.-jun: 2019. ilus
Article in Spanish | LILACS-Express | LILACS | ID: biblio-1014514

ABSTRACT

Herlyn-Werner-Wunderlich syndrome is a rare congenital anomaly of the urogenital tract caused by defective fusion of the Müllerian ducts, which gives rise to obstructed hemivagina, uterus didelphys and ipsilateral renal agenesis. We report the case of a 16-year-old girl who underwent resection of the vaginal septum and drainage of the secondary hematocolpos, thus preserving her reproductive function.


El síndrome de Herlyn-Werner-Wunderlich es una anomalía congénita rara del tracto urogenital, causada por un fallo de la fusión de los conductos müllerianos, que se caracteriza por presentar una hemivagina obstruida, útero didelfo y anomalía renal ipsilateral. Presentamos el caso de una paciente de 16 años a quien se le realizó resección del tabique vaginal y drenaje del hematocolpos secundario, para así preservar su función reproductiva.

3.
Childhood Kidney Diseases ; : 124-127, 2019.
Article in English | WPRIM | ID: wpr-785572

ABSTRACT

Herlyn-Werner-Wunderlich (HWW) syndrome is a rare congenital anomaly of the genitourinary tract comprising uterus didelphys, obstructed hemivagina, and ipsilateral renal agenesis. Patients with HWW syndrome usually present symptoms such as dysmenorrhea, abdominal pain, pelvic mass, and purulent vaginal discharge. If not treated at an appropriate time, complications such as infertility, endometriosis, pyosalpinx, and subsequent pelvic adhesions may occur. Here, we report a case of HWW syndrome in a 7-year-old-girl who was also diagnosed as having central precocious puberty. She was brought to the pediatric department with chief complaints of lump in her breast and vaginal discharge. When she was around 2 months old, she was confirmed to have a single kidney on ultrasonography. We checked her past medical history and diagnosed her as having HWW syndrome based on the results of imaging studies, including abdominal ultrasonography and pelvic magnetic resonance imaging. She underwent treatment with gonadotropin-releasing hormone analogue for 2 years. During 24 months of follow-up, she showed no serious problems or complications. If renal anomalies are identified immediately after birth or in infancy, further screening tests should be conducted prior to menstruation for determining congenital abnormalities of the reproductive tract and vice versa.


Subject(s)
Abdominal Pain , Breast , Congenital Abnormalities , Dysmenorrhea , Endometriosis , Female , Follow-Up Studies , Gonadotropin-Releasing Hormone , Humans , Infertility , Kidney , Magnetic Resonance Imaging , Mass Screening , Menstruation , Parturition , Puberty, Precocious , Ultrasonography , Uterus , Vaginal Discharge
4.
Article in Chinese | WPRIM | ID: wpr-706316

ABSTRACT

Objective To observe imaging features of uterus duplication combined with mesonephric duct dysplasia related abnormalities.Methods Imaging data of 17 female with uterus duplication and renal dysplasia were retrospectively analyzed.Seven patients underwent CT and 10 patients underwent MR scanning.Results The basic abnormalities in 17 patients were uterus duplication combined with unilateral renal-ureter dysplasia with/without other associated malformation which were further classified as follows:①7 patients presented as basic abnormalities without other associated malformations,include 5 (CT diagnosed 1,MR diagnosed 4) with uterus duplex and unilateral renal-ureter agenesis,2 (CT 1,MR 1) with uterus bifidus and unilateral renal-ureter dysplasia;②2 patients (CT 1,MR 1) presented as basic abnormalities accompanied with ectopic ureter orifice,uterus duplex and unilateral renal dysplasia with ectopic ureter orifice opening in vagina;③5 patients (CT 3,MR 2) of Herlyn-Werner-Wunderlich syndrome presented as uterus duplication,oblique vagina septum as well as unilateral renal-ureter dysplasia,which shown as uterus duplex,oblique vaginal septum with hematocolpos,also unilateral renal-ureter agenesis;④2 patients presented as basic abnormalities accompanied with mesonephric residual cyst,CT showed one with uterus duplex and unilateral renal-ureter agenesis with ipsilateral mesonephric residual cyst,MRI showed as the other one with Herlyn-Werner-Wunderlich syndrome combined with mesonephric residual cyst opening in vagina;⑤MRI showed 1 patient with basic abnormalities and a nephrogenic adenoma,which demonstrated as uterus duplex combined with left renal-ureter agenesis,and a tumor on the left wall of bladder accompanied with endometriosis.Conclusion Further classification into 5 types from simple to complex based on uterus duplication combined with unilateral renal-ureter dysplasia with/without other associated malformations is helpful to the diagnosis and treatment of these abnormalities.

5.
Article in English | WPRIM | ID: wpr-739188

ABSTRACT

Herlyn-Werner-Wunderlich (HWW) syndrome is a rare congenital malformation syndrome that is characterized by a triad of uterine didelphys, blind hemivagina, and ipsilateral renal agenesis. There is a wide variety of phenotypic presentation which is recognized as a spectrum of disease rather than a separate entity. The exact incidence and pathogenesis of HWW syndrome are yet to be investigated. While this disease typically involves adolescent girls who present with abdominal pain or a pelvic mass that is secondary to hematocolpos, nowadays, a majority of potential patients with HWW are being prenatally screened for renal anomalies. Therefore, it is recommended to search for uterovaginal anomalies whenever a multicystic dysplastic kidney or the absence of a kidney is noted in a newborn female, and the role of pediatric nephrologists has become ever more important for early recognition of the disease.


Subject(s)
Abdominal Pain , Adolescent , Female , Hematocolpos , Humans , Incidence , Infant, Newborn , Kidney , Multicystic Dysplastic Kidney
6.
National Journal of Andrology ; (12): 452-454, 2017.
Article in Chinese | WPRIM | ID: wpr-812743

ABSTRACT

Objective@#To explore the clinical diagnosis and treatment of seminal vesicle cyst (SVC) associated with ipsilateral renal agenesis (Zinner syndrome) in order to promote the understanding of the disease.@*METHODS@#We retrospectively analyzed the clinical data about 1 case ofZinner syndrome diagnosed and treated in our hospital and reviewed the literature related to this disease in domestic and foreign authoritative databases.@*RESULTS@#The patient was a 23-year-old male, diagnosed with Zinner syndrome, treated bytransrectal aspiration of SVC, and discharged from hospital 3 days postoperatively. Follow-upat 6 months after discharge found that the patient no longer felt perineal discomfort in the endstage of urination, but transrectal ultrasonography of the prostate revealedthe samevolume of fluid in the left seminal vesicles as before,which indicated recurrence.@*CONCLUSIONS@#SVC associated with ipsilateral renal agenesis can be considered asZinner syndrome. Transrectal aspiration of SVCcan relieve the local symptoms of the patient but relapse may easilyoccur. Therefore it is not recommended as the first-choice treatment of the disease.


Subject(s)
Cysts , Diagnostic Imaging , Therapeutics , Genital Diseases, Male , Diagnostic Imaging , Therapeutics , Humans , Male , Perineum , Recurrence , Retrospective Studies , Seminal Vesicles , Diagnostic Imaging , Solitary Kidney , Syndrome , Ultrasonography , Young Adult
7.
Article in English | WPRIM | ID: wpr-110655

ABSTRACT

Herlyn-Werner-Wunderlich syndrome is a rare congenital anomaly of the urogenital tract, which is characterized by the triad of uterus didelphys, obstructed hemivagina, and ipsilateral renal agenesis. It usually presents at puberty with pelvic pain, dysmenorrhea, and a vaginal or pelvic mass. Although rare, it may present with purulent vaginal discharge due to secondary infection of the obstructed hemivagina, making diagnosis difficult. A careful pelvic examination to identify the cervix and vagina is the key to the diagnosis of Müllerian duct anomalies and magnetic resonance imaging can provide additional useful information. The optimal treatment is full excision and marsupialization of the obstructing vaginal septum so that both uteri can drain through the patent vagina. The authors report a case of a 22-year-old female with an unusual presentation of Herlyn-Werner-Wunderlich syndrome complicated by pyocolpos, which was successfully managed by vaginal septum resection and drainage of pus.


Subject(s)
Adolescent , Cervix Uteri , Coinfection , Diagnosis , Drainage , Dysmenorrhea , Female , Gynecological Examination , Humans , Magnetic Resonance Imaging , Pelvic Pain , Puberty , Suppuration , Uterus , Vagina , Vaginal Discharge , Young Adult
8.
Neonatal Medicine ; : 49-52, 2017.
Article in English | WPRIM | ID: wpr-32563

ABSTRACT

Smith-Magenis syndrome (SMS) is a genetic disease caused by microdeletion of p11.2 in chromosome 17. SMS patients have characteristic facial features and accompanying congenital malformations involving the brain, cardiovascular system, and urinary tract. Compared with the distinctive facial characteristics, organ malformations are less common. Several cases of SMS with tetralogy of Fallot have been reported in Korea, none of which were accompanied by other organ malformations. We present the first case report in Korea of an SMS patient with malformations of the brain, heart, and urinary tract.


Subject(s)
Brain , Cardiovascular System , Chromosomes, Human, Pair 17 , Cisterna Magna , Heart , Humans , Korea , Smith-Magenis Syndrome , Tetralogy of Fallot , Urinary Tract
9.
Int. braz. j. urol ; 42(4): 842-844, July-Aug. 2016. graf
Article in English | LILACS | ID: lil-794691

ABSTRACT

ABSTRACT Associated congenital anomalies are seen in 21% of retrocaval ureter patients; among them, associated contralateral renal agenesis is a very rare entity. We report one such case of right circumcaval ureter with left renal agenesis, diagnosed after febrile UTI. Surgical correction with uretero-ureterostomy was successful. In literature very few such cases are reported and only one case with renal failure was reported. Unilateral renal agenesis cases complicated by associated such anomalies need definitive management and lifelong clinical monitoring to diagnose and prevent chronic kidney disease.


Subject(s)
Humans , Male , Female , Adult , Congenital Abnormalities/diagnostic imaging , Retrocaval Ureter/diagnostic imaging , Kidney/abnormalities , Kidney Diseases/congenital , Ureter/surgery , Vena Cava, Inferior , Tomography, X-Ray Computed , Retrocaval Ureter/surgery , Hydronephrosis/diagnostic imaging , Kidney/diagnostic imaging , Kidney Diseases/diagnostic imaging
10.
Article in English | IMSEAR | ID: sea-178747

ABSTRACT

Background & objectives: The role of cystic fibrosis transmembrane conductance regulator (CFTR) gene mutations in congenital bilateral absence of vas deferens and unilateral renal agenesis (CBAVD-URA) has been controversial. Here, we report the cases of five Indian males with CBAVD-URA. The objective was to evaluate the presence or absence of CFTR gene mutations and variants in CBAVD-URA. The female partners of these males were also screened for cystic fibrosis (CF) carrier status. Methods: Direct DNA sequencing of CFTR gene was carried out in five Indian infertile males having CBAVD-URA. Female partners (n=5) and healthy controls (n=32) were also screened. Results: Three potential regulatory CFTR gene variants (c.1540A>G, c.2694T>G and c.4521G>A) were detected along with IVS8-5T mutation in three infertile males with CBAVD-URA. Five novel CFTR gene variants (c.621+91A>G, c.2752+106A>T, c.2751+85_88delTA, c.3120+529InsC and c.4375-69C>T), four potential regulatory CFTR gene variants (M470V, T854T, P1290P, Q1463Q) and seven previously reported CFTR gene variants (c.196+12T>C, c.875+40A>G, c.3041-71G>C, c.3271+42A>T, c.3272-93T>C, c.3500-140A>C and c.3601-65C>A) were detected in infertile men having CBAVD and renal anomalies Interpretation & conclusions: Based on our findings, we speculate that CBAVD-URA may also be attributed to CFTR gene mutations and can be considered as CFTR-related disorder (CFTR-RD). The CFTR gene mutation screening may be offered to CBAVD-URA men and their female partners undergoing ICSI. Further studies need to be done in a large sample to confirm the findings.

11.
Article in Korean | WPRIM | ID: wpr-148714

ABSTRACT

Herlyn-Werner-Wunderlich (HWW) syndrome is a rare, congenital genitourinary anomaly involving the Müllerian and Wolffian structures, and is characterized by the triad of uterine didelphys, obstructed hemivagina, and ipsilateral renal agenesis. It usually presents in adolescent girls in whom hematometrocolpos produces a pronounced mass effect and pain on the side of the obstructed hemivagina. Accurate diagnosis and surgical treatment can be delayed for several months or even years. Here, we report a case of a 12-year-old girl who presented to the emergency department with lower abdominal pain and mass that had lasted for 2 weeks. After the confirmation of HWW syndrome with magnetic resonance imaging, hysteroscopic septostomy was carried out as a definitive treatment. When we evaluate adolescent girls with lower abdominal pain and mass, we should consider the possibility of HWW syndrome.


Subject(s)
Abdominal Pain , Adolescent , Child , Diagnosis , Emergency Service, Hospital , Female , Hematocolpos , Humans , Magnetic Resonance Imaging , Mullerian Ducts , Wolffian Ducts
12.
Article in English | IMSEAR | ID: sea-165822

ABSTRACT

Background: Congenital anomalies of urinary system are common and are found in 3-4% of population, and lethal urinary anomalies account for 10% of termination of pregnancy. Methods: A study was done to know the incidence of congenital anomalies at birth for the period of 4 months from May 99 - Sept 99 at Cheluvamba hospital attached to Mysore medical college. Congenital anomalies in the still births, live births and aborted fetuses >20 weeks were studied along with the case history and ultrasound reports. Aborted fetuses and still born babies were collected for autopsy after the consent of parents. These babies were fixed in 10% formalin and autopsy was done after fixing, and anomalies were noted. Results: Total births during study period were 3000. There were 61 babies with congenital anomalies and 6 babies had anomalies of urinary system. Among the urinary system anomalies 1 baby had bilateral renal agenesis, 1 baby had unilateral renal agenesis with anophthalmia (Fraser syndrome), 2 babies had Multicystic dysplastic kidney disease (MCDK) and 1 live baby had hydronephrosis due to obstruction at pelvi ureteric junction, and 1 live female baby had polycystic kidneys. Conclusion: Incidence of urinary system anomalies in the present study was 2 per 1000 births. U/S detection of urinary anomalies varies with period of gestation, amniotic fluid volume and visualisation of urinary bladder. Autopsy helps to detect renal agenesis.

13.
Article in English | IMSEAR | ID: sea-156771

ABSTRACT

In the embryo, the limb arises as a condensation of cells from the lateral plate mesoderm and its Ectodermal covering. Congenital malformations involving limb sometimes lead to prenatal mortality, post natal morbidity and psychological effect on parents. Polymelia is one of such condition where diagnostic decisiveness rest on shoulder of radiologist and has an implication on management aspect as far as surgery is concern. We report one unique case having polymelia with left renal agenesis.

14.
Chinese Journal of Radiology ; (12): 480-483, 2014.
Article in Chinese | WPRIM | ID: wpr-451283

ABSTRACT

Objective To explore imaging features of Zinner syndrome.Methods Eight male patients with clinically diagnosed Zinner syndrome performed abdominal and pelvic CT and /or MRI scan.The radiological data was studied retrospectively.Results Eight cases showed seminal vesicle cyst with ipsilateral renal agenesis on CT and/or MR imaging ( left side, n =5; right side, n =3).The maximal diameter of seminal vesicle cysts varied from 4.2 to 7.0 cm, and appeared as oval cystic lesion with irregular contour or tube-like dilatation , which appeared low density on CT image and hypo-or hyperintensity on T 1 WI and hyperintensity on T 2 WI.Bladder compression was found in 6 cases.Fuild-fuild level in the cysts was seen in 2 cases.Remnants of ureter structure were seen in only 1 case.There was no other accompanying abnormality of urinary system.Conclusions Zinner syndrome presents with characteristic imaging features , and the key issue is differential diagnosis of seminal vesicle cysts.

15.
Article in English | WPRIM | ID: wpr-37130

ABSTRACT

Most cases of double uterus with obstructed hemivagina and ipsilateral renal agenesis were diagnosed at adolescents after menarche. This is the first reported case of complete septate uterus with obstructed hemivagina and ipsilateral renal agenesis in addition to ipsilateral agenesis of fallopian tube and ovary in which the diagnosis was delayed until pregnancy. The pregnancy was uneventful in spite of intermittent vaginal spotting. During the cesarean section, the septum of the uterus was resected and about a 3-cmx3-cm window was made on the vaginal septum to allow an opening for the obstructed vaginal discharge. We followed the patient up for one and half years, and she has not had symptoms such as dysmenorrhea or abnormal vaginal bleeding.


Subject(s)
Adolescent , Cesarean Section , Diagnosis , Dysmenorrhea , Fallopian Tubes , Female , Humans , Menarche , Metrorrhagia , Ovary , Pregnancy , Uterine Hemorrhage , Uterus , Vaginal Discharge
16.
Indian J Hum Genet ; 2013 Jan; 19(1): 113-115
Article in English | IMSEAR | ID: sea-147650

ABSTRACT

Mayer-Rokitansky-Kuster-Hauser (MRKH) is a malformation complex comprising absent vagina and absent or rudimentary uterus. MRKH syndrome may be attributed to an initial affection of the intermediate mesoderm consequently leading (by the end of the 4th week of fetal life) to an alteration of the blastema of the cervicothoracicsomites and the pronephricducts. These latter subsequently induce the differentiation of the mesonephric and then the Wolffian and Mullerian ducts. There are very sparse such cases reported. We present a case of type II MRKH or Mullerian renal cervical somite association (i.e., Mullerian duct aplasia, renal dysplasia, and cervical somite anomalies).


Subject(s)
46, XX Disorders of Sex Development/epidemiology , Abnormalities, Multiple , Adult , Congenital Abnormalities , Dandy-Walker Syndrome/epidemiology , Dandy-Walker Syndrome/genetics , Female , Humans , Kidney/abnormalities , Kidney Diseases/congenital , Mullerian Ducts/abnormalities
17.
Neonatal Medicine ; : 159-166, 2013.
Article in Korean | WPRIM | ID: wpr-24375

ABSTRACT

Herlyn-Werner-Wunderlich syndrome (HWWS) is a very rare congenital anomaly of the urogenital tract involving Mullerian ducts and Wolffian ducts, and is characterized by the triad of uterine didelphys, unilateral obstructed hemivagina and ipsilateral renal agenesis. Generally it is diagnosed at puberty after menarche due to recurrent pelvic pain or abdominal mass. We report 2 cases of female newborns whose fetal ultrasonography (USG) showed unilateral renal agenesis and were diagnosed with HWWS by postnatal evaluation. Both cases were female newborns who were born at term by vaginal delivery. They had no perinatal problems except suspicious findings of unilateral renal agenesis from fetal USG. Abdominal ultrasonography and pelvic MRI were performed after birth, and they were diagnosed with HWWS. The potential complications of this syndrome such as pyosalpinx, pelvic adhesions and increased risk of abortion or infertility can occur, but without complication, the prognosis is very good with simple surgical treatment. If renal agenesis is detected in a fetus or a newborn, possible anomalies of urogenital tract such as HWWS should be considered; and postnatal evaluation should be performed, as a simple surgical treatment before menarche can prevent unnecessary complications of disease.


Subject(s)
Congenital Abnormalities , Female , Fetus , Humans , Infant, Newborn , Infertility , Kidney , Kidney Diseases , Menarche , Mullerian Ducts , Parturition , Pelvic Pain , Prognosis , Puberty , Ultrasonography, Prenatal , Urogenital Abnormalities , Wolffian Ducts
18.
Gac. méd. boliv ; 35(2): 80-83, dic. 2012. ilus, graf, tab
Article in Spanish | LILACS | ID: lil-737872

ABSTRACT

La sirenomelia constituye una anomalía congénita infrecuente, cuya característica principal es la fusión de las extremidades inferiores; la etiología es aún desconocida, sin embargo existen varias teorías planteadas para determinar el origen de esta entidad rara. Es de difícil diagnóstico prenatal, ya que por lo general se asocia a oligoamnios. Las malformaciones asociadas son muy variables, pero por lo general incompatibles con la vida, por lo tanto el pronóstico es sombrío. En el siguiente artículo se reporta un caso clínico de un recién nacido con sirenomelia, en el Hospital Obrero N°2 de la Caja Nacional de Salud, que debido a la asociación de agenesia renal bilateral, presenta un mal pronóstico y fallece a las ocho horas de vida.


The sirenomelia is a rare congenital anomaly, whose main characteristic is the fusion of the lower extremities, the etiology is still unk-nown, but there are several theories raised to determine the origin of this rare entity. Prenatal diagnosis is difficult, and usually is asso-ciated with oligohydramnios. Associated malformations are highly variable, but usually incompatible with life, so the prognosis is poor. The following article reports a case of a newborn with sirenomelia, Hospital Obrero N°2 de la Caja Nacional de Salud, that due to the association of bilateral renal agenesis, has a poor prognosis and died within eight hours of life.


Subject(s)
Ectromelia
19.
Rev. Fac. Med. (Caracas) ; 35(1): 52-54, ene.-jun. 2012. ilus
Article in Spanish | LILACS | ID: lil-682988

ABSTRACT

Las malformaciones müllerianas tienen una incidencia mundial de 0,1 % a 0,5 %, siendo en Venezuela de 0.02 %; se asocia de 37 % a 60 % con agenesia renal congénita. Se ha observado que la relación entre malformación mülleriana y agenesia renal aumentan la incidencia de trastornos hipertensivos del embarazo. Se presenta el caso de una paciente de 18 años, IIG, IP, con embarazo de 30 semanas más 2 días por FUR, con diagnóstico de útero bicorne y agenesia renal, quien ingresó con presión arterial elevada, durante su hospitalización presentó proteinuria y síntomas neurológicos. Se diagnosticó preeclampsia grave y se interrumpió el embarazo. La evolución de madre e hijo fue normal, la madre egresó a los tres días y el recién nacido al mes. No encontramos en la literatura venezolana casos similares, por lo que este constituye el primero reportado


Müllerian malformations have a global incidence of 0.1 % to 0.5 %, in Venezuela the incidence is close to 0.02 %; is associated in 37 % to 60% with congenital renal agenesis. It has been observed that the relationship between renal agenesis and Mullerian malformation increases the incidence of hypertensive disorders of pregnancy. We present a case of 18 years old patient of 18, IIG, IP, with a pregnancy of 30 weeks plus 2 days by LMP, diagnosed with bicornuate uterus and renal agenesis, who was admitted with high blood pressure, during hospitalization showed proteinuria and neurological symptoms. Severe preeclampsia was diagnosed and pregnancy termination performed. The mother and child outcome was satisfactory, the mother was discharged after three days and the baby a month. We did not found in the Venezuelan literature similar cases, so this is the first reported


Subject(s)
Humans , Female , Pregnancy , Adolescent , Congenital Abnormalities/diagnosis , Hypertension, Pregnancy-Induced/pathology , Pre-Eclampsia/pathology , DiGeorge Syndrome/diagnosis , Uterus/abnormalities , Obstetrics , Pregnancy Complications
20.
Article in English | WPRIM | ID: wpr-203009

ABSTRACT

Seminal vesicle cyst (SVC) with ipsilateral renal agenesis is a rare congenital anomaly. When the patient is symptomatic, surgical treatment may be necessary. The open surgical approach, traditionally considered the definite form of treatment, has been associated with a high rate of morbidity. The laparoscopic approach for the management of SVCs has recently been described. A 18-year-old man presented with a 2-year history of dysuria and perineal pain. The diagnostic evaluation revealed a 45x35x48 mm sized left seminal vesicle cyst. In addition, he had a solitary, right, functioning kidney, with left renal agenesis. Transperitoneal laparoscopic excision of the cyst was performed successfully. The patient was discharged from the hospital on the fourth postoperative day and did not present with any complaints or complications.


Subject(s)
Adolescent , Congenital Abnormalities , Dysuria , Humans , Kidney , Kidney Diseases , Seminal Vesicles
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