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1.
Pediatr Surg Int ; 38(11): 1649-1655, 2022 Nov.
Artículo en Inglés | MEDLINE | ID: mdl-35964259

RESUMEN

PURPOSE: Antenatal auto-amputation of the ovary is an extremely rare event, and its diagnosis is difficult. We aimed to retrospectively review the cases with antenatal auto-amputation, where the diagnosis was made based on detection of free-floating cyst during surgery. METHODS: Patients diagnosed with auto-amputated ovary during the surgery between 2012 and 2021 were included in the study. The data were reviewed retrospectively. Clinical, radiological, surgical, and histopathological findings were recorded. RESULTS: Eight patients underwent surgery for an abdominal cystic mass. The age range of patients who were operated was from 21 days to 9 months. None of the patients had symptoms, except one patient who had a large cyst and was vomiting. Prenatal ultrasound examination indicated an intra-abdominal cyst in all patients, but auto-amputated ovary diagnosis was not made. Differential postnatal diagnoses included an ovarian cyst, ovarian teratoma, tuba-ovarian torsion, mesenteric lymphatic malformation, and intestinal duplication cyst. Only one patient had an auto-amputated ovary suspicion in computed tomography. Laparoscopic exploration (n: 7) or laparotomy (n: 1) was performed. Histopathologic examination was necrosis and calcification (n: 6), necrosis (n: 1), and serous cystadenoma and necrosis (n: 1). CONCLUSION: We suggest that laparoscopy should be used for diagnosis and treatment of antenatal intra-abdominal cysts that persist postnatally because of diagnostic dilemmas. We recommend in patients diagnosed with auto-amputated ovary that the other ovary should be carefully monitored and followed up in terms of ovarian cyst, due to the possible risk of torsion.


Asunto(s)
Quistes , Laparoscopía , Quistes Ováricos , Quistes/cirugía , Femenino , Humanos , Lactante , Recién Nacido , Necrosis/cirugía , Quistes Ováricos/diagnóstico por imagen , Quistes Ováricos/cirugía , Embarazo , Estudios Retrospectivos , Anomalía Torsional/diagnóstico por imagen , Anomalía Torsional/cirugía
2.
Ulus Travma Acil Cerrahi Derg ; 28(4): 464-470, 2022 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-35485519

RESUMEN

BACKGROUND: Priapism is a rare condition in children and the treatment algorithm is controversial in this age group. Herein, we report eight cases with low-flow priapism and our stepwise treatment approach in light of literature. METHODS: We present a simple stepwise treatment for low-flow priapism including five steps. Step 1: Cold compress and analgesia while evaluation the priapism and its etiology. Step 2: Corporal aspiration and adrenaline infusion in the ward. Step 3: Modified Winter shunt in the same place. Step 4: Ketamine application and caudal block in the operating room. Step 5: Sapheno-cavernous (Grayhack) shunt. Eight cases with low-flow priapism were reviewed retrospectively. Symptoms, duration of tumescence, the interventions, and step that provide detumescence were recorded. RESULTS: The mean age of patients was 8.5 years (1-17 y). The median time of the priapism before admission was 15 h (4-165 h). The etiological factors were sickle cell disease, hemodialysis due to chronic renal failure, and factor V Leiden mutation in three patients. Detumescence was achieved in one patient at Step 2, in two patients at Steps 3, 4, and 5, respectively. Rigidity of cavernous body was observed in one patient in long-term follow-up. CONCLUSION: Low-flow priapism is a urological emergency that may cause erectile dysfunction. Treatment options should be selected according to a protocol that prevents time loss and avoids more invasive treatment in unnecessary situations. Our algorithm with simple nature and its steps from less invasive to more invasive procedures may be an alternative for the treatment of low-flow priapism.


Asunto(s)
Disfunción Eréctil , Priapismo , Niño , Disfunción Eréctil/complicaciones , Humanos , Masculino , Manejo del Dolor , Priapismo/cirugía , Priapismo/terapia , Estudios Retrospectivos
3.
Pediatr Hematol Oncol ; 35(3): 208-217, 2018 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-30346857

RESUMEN

INTRODUCTION: The aim of this study is to evaluate late side effects that affect quality of life in children with sacrococcygeal teratoma (SCT). PATIENTS AND METHODS: The patients with SCT were evaluated retrospectively. The data were expressed by percentage and the subgroups were compared statistically. RESULTS: A total of 40 children with SCT were identified with median age 12 days (range: 1 day-14.6 years), 27 of whom were analyzed in this study with urodynamic data available for 24 and anal manometric evaluations for 20. Chronic constipation with need for laxative was reported in (7/27) 25.9%, fecal incontinence was present in (1/27) 3.7%, and urodynamic abnormalities were reported in (16/24) 66%. Among those with urodynamic abnormalities, low bladder capacity, dyssyergia and neurogenic bladder were observed in (21/24) 87.5% and anticholinergic treatment was applied. Urinary incontinence was present in (2/27) 7%, with clean intermittent catheterization utilized in (7/27) 25.9%. While defecation was observed more in the patients with Altman types II, III, and IV, micturation problems were observed more in the patients with Altman types II and IV. It was found that urodynamic dysfunctions were more frequent in the patients with increased number of operations. DISCUSSION: Although the rate of symptomatic patients was low, abnormalities determined by radiological and urodynamic evaluations were high.


Asunto(s)
Recurrencia Local de Neoplasia/etiología , Complicaciones Posoperatorias , Región Sacrococcígea/cirugía , Teratoma/cirugía , Trastornos Urinarios/etiología , Procedimientos Quirúrgicos Urológicos/efectos adversos , Adolescente , Niño , Preescolar , Femenino , Estudios de Seguimiento , Humanos , Lactante , Masculino , Recurrencia Local de Neoplasia/diagnóstico , Pronóstico , Calidad de Vida , Estudios Retrospectivos , Región Sacrococcígea/patología , Teratoma/patología , Trastornos Urinarios/diagnóstico
4.
Int Urol Nephrol ; 50(8): 1367-1373, 2018 Aug.
Artículo en Inglés | MEDLINE | ID: mdl-29968144

RESUMEN

OBJECTIVE: We aimed to evaluate the efficacy and safety of intravesical onabotulinum toxin A (onaBoNTA) injections for the treatment of children diagnosed with refractory overactive bladder (OAB) by using non-invasive methods. METHODS: A total of 31 pediatric patients with a mean age of 10.2 years received intravesical onaBoNTA injection at the dose of 10 U/kg (max: 200 U). Twenty-one patients who failed to respond to the first injection, received second injection 6 months after the first one. The patients were retrospectively evaluated after the 1st and the 2nd injections by means of standardized questionnaire forms and voiding diary records. RESULTS: In the 6-month follow-up, 10 patients (32.2%) were determined to have full response after the first injection. The number of patients with partial response and no response were found to be 15 (48.4%) and 6 (19.4%), respectively. The mean value of Dysfunctional Voiding and Incontinence Symptom Score (DVISS) of the patients with full response was 8.5 before the injection, which decreased to 1 at 6-month follow-up and to 0.5 at 12-month follow-up (p < 0.001). Twenty-one patients without full response after the first injection received a second injection 6 months after the first one. Full response was achieved in 9 (42.9%) of the 21 patients who had a second injection, but only partial response was achieved in 9 (42.9%). Three (14.3%) of the remaining patients did not respond to the second injection either. 1-year follow-up evaluations revealed that the rates of the full response, partial response, and no response were 61.3, 29, and 9.7%, respectively. CONCLUSIONS: Based on our results, onaBoNTA therapy is an effective and reliable second-line off-label therapy in the management of patients with non-neurogenic OAB that is refractory to medical therapy. Asking the patients/guardians to fill out a standardized questionnaire form before and after the therapy enables easy and non-invasive assessment of the response to the therapy.


Asunto(s)
Toxinas Botulínicas Tipo A/administración & dosificación , Vejiga Urinaria Hiperactiva/tratamiento farmacológico , Micción/fisiología , Administración Intravesical , Adolescente , Niño , Relación Dosis-Respuesta a Droga , Femenino , Estudios de Seguimiento , Humanos , Masculino , Fármacos Neuromusculares/administración & dosificación , Estudios Retrospectivos , Factores de Tiempo , Resultado del Tratamiento , Vejiga Urinaria Hiperactiva/fisiopatología
5.
Balkan Med J ; 35(3): 268-271, 2018 05 29.
Artículo en Inglés | MEDLINE | ID: mdl-29148427

RESUMEN

Background: Urothelial carcinoma of the bladder is a rare condition in children, and most cases in this age group are noninvasive and low-grade. However, no follow-up protocol has been defined for this patient group. The objective of this study was to draw attention to bladder tumors in children and focus on the current recommendations for postoperative follow-up along with a case study of four patients. Case Report: Four patients aged <18 years with urothelial carcinoma who were treated in our clinics between 2001 and 2015 were retrospectively evaluated. The results were compared with those of published pediatric case series in the literature. No abnormalities were found in the patients' physical examinations and laboratory analyses, except hematuria (microscopic or macroscopic). Ultrasonography was used in all the patients to detect lesions in the bladder. Surgical resections were performed endoscopically, except in one patient. Histopathological evaluations revealed low-grade superficial urothelial carcinoma. No recurrence or complication was observed for all patients. Conclusion: Although rarely encountered during childhood, urothelial carcinoma should be considered as a differential diagnosis in pediatric patients with hematuria.


Asunto(s)
Carcinoma de Células Transicionales/diagnóstico , Neoplasias de la Vejiga Urinaria/diagnóstico , Adolescente , Carcinoma de Células Transicionales/diagnóstico por imagen , Carcinoma de Células Transicionales/cirugía , Niño , Femenino , Hematuria/diagnóstico , Humanos , Masculino , Recurrencia Local de Neoplasia , Estudios Retrospectivos , Resultado del Tratamiento , Ultrasonografía , Neoplasias de la Vejiga Urinaria/diagnóstico por imagen , Neoplasias de la Vejiga Urinaria/cirugía
6.
Balkan Med J ; 34(6): 572-575, 2017 12 01.
Artículo en Inglés | MEDLINE | ID: mdl-29215339

RESUMEN

BACKGROUND: Urethral duplication and megalourethra are rare urethral anomalies. However, the concomitance of urethral duplication and double megalourethra has not been reported previously. CASE REPORT: A newborn was presented with penile swelling during voiding. Physical examination revealed a retractable foreskin and two external meatus of a double urethra. Retrograde urethrography demonstrated two complete megalourethras. Urethro-urethrostomy and urethroplasty were performed when the patient was 10 months old. The patient was followed up for one year without any urinary problems and has good cosmetics and urinary continence. CONCLUSION: The concomitance of these two rare anomalies and more importantly its surgical treatment makes this case report unique and valuable.


Asunto(s)
Uretra/anomalías , Uretra/cirugía , Enfermedades Uretrales/cirugía , Trastornos Urinarios/cirugía , Procedimientos Quirúrgicos Urológicos , Anomalías Múltiples/diagnóstico por imagen , Anomalías Múltiples/fisiopatología , Anomalías Múltiples/cirugía , Estudios de Seguimiento , Humanos , Recién Nacido , Masculino , Enfermedades Raras , Resultado del Tratamiento , Uretra/diagnóstico por imagen , Uretra/fisiopatología , Enfermedades Uretrales/diagnóstico por imagen , Enfermedades Uretrales/fisiopatología , Trastornos Urinarios/diagnóstico por imagen , Trastornos Urinarios/fisiopatología , Urografía
7.
Int J Urol ; 13(2): 105-8, 2006 Feb.
Artículo en Inglés | MEDLINE | ID: mdl-16563131

RESUMEN

BACKGROUND: Treatment with anticholinergic agents is the mainstay of therapy for detrusor instability (DI), a chronic and morbid condition characterized by urge urinary incontinence. The aim of this study is to assess the effectiveness and tolerability of tolterodine and oxybutynin in children with DI. METHODS: A total of 60 children with DI were enrolled, 30 (14 male, 16 female, mean age 7.97+/-2.71 years) in the tolterodine group and 30 (12 male, 18 female, mean age 7.33+/-2.23 years) in the oxybutynin group. In this prospective study we reviewed data from 60 children followed for at least 6 months. All of the patients in the study population had a history of dysfunctional voiding. Urodynamic investigations were conducted in all of the patients before and after anticholinergic treatment. Episodes of urge urinary incontinence and adverse events were also evaluated. RESULTS: Improvements in urge incontinence episodes were similar for the children who received tolterodine or oxybutynin. Improvements in the urodynamic parameters were also the same in the two groups. Adverse events were significantly lower in the tolterodine group (13 events in 13 patients) compared to the oxybutynin group (27 events in 20 patients; P=0.027). CONCLUSION: Reductions in urge urinary incontinence episodes were similar with tolterodine and oxybutynin in children with DI. Side-effects were more common with oxybutynin. Treatment of children with DI with tolterodine shows significantly better tolerability and this may enhance children's compliance during long-term treatment.


Asunto(s)
Compuestos de Bencidrilo/uso terapéutico , Cresoles/uso terapéutico , Ácidos Mandélicos/uso terapéutico , Antagonistas Muscarínicos/uso terapéutico , Fenilpropanolamina/uso terapéutico , Incontinencia Urinaria/tratamiento farmacológico , Compuestos de Bencidrilo/efectos adversos , Niño , Preescolar , Cresoles/efectos adversos , Femenino , Humanos , Masculino , Ácidos Mandélicos/efectos adversos , Antagonistas Muscarínicos/administración & dosificación , Fenilpropanolamina/efectos adversos , Estudios Prospectivos , Tartrato de Tolterodina , Incontinencia Urinaria/fisiopatología
8.
Urol Int ; 74(4): 373-6, 2005.
Artículo en Inglés | MEDLINE | ID: mdl-15897709

RESUMEN

In this study, we report a 3-year-old boy with severe scrotal hypospadias with Robertsonian translocation [45,XY,t(13q;14q)]. The patient was born at term with a low birth weight and hypospadias. There was no endocrinological abnormality. His father also has a balanced 13-14 Robertsonian translocation. Two-stage hypospadias repair was carried out. The presence of this chromosomal anomaly and hypospadias are unique to our patient, compared to others with the 45,XY,t(13q;14q) translocation. Although no such association has been reported so far, we thought that severe hypospadias in this case might be associated with this translocation.


Asunto(s)
Hipospadias/genética , Translocación Genética/genética , Anomalías Urogenitales/genética , Preescolar , Aberraciones Cromosómicas , Enfermedades Genéticas Congénitas/complicaciones , Enfermedades Genéticas Congénitas/genética , Predisposición Genética a la Enfermedad , Humanos , Hipospadias/complicaciones , Hipospadias/cirugía , Masculino , Resultado del Tratamiento , Anomalías Urogenitales/complicaciones , Anomalías Urogenitales/cirugía , Procedimientos Quirúrgicos Urológicos Masculinos
9.
Int J Urol ; 12(3): 311-2, 2005 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-15828962

RESUMEN

Computed tomography is a very useful diagnostic tool in children's trauma. In the present case report, retrograde filling of the renal vein during computerized tomographic examination of a patient with renal trauma is presented. This is an indirect sign of traumatic renal artery injury. This finding might assist in the early diagnosis of severe renovascular trauma.


Asunto(s)
Riñón/lesiones , Arteria Renal/lesiones , Tomografía Computarizada por Rayos X , Traumatismos Abdominales/etiología , Accidentes de Tránsito , Niño , Humanos , Masculino , Cintigrafía , Venas Renales/diagnóstico por imagen , Ultrasonografía Doppler en Color , Heridas no Penetrantes/complicaciones
10.
Int J Urol ; 12(3): 316-8, 2005 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-15828964

RESUMEN

Tumors of the urinary bladder are rare in children and nearly all of them are of mesodermal in origin. Herein we report a case of transitional cell carcinoma of the urinary bladder in a 13-year-old boy who presented after blunt abdominal trauma. It should be remembered that hematuria could develop after blunt abdominal trauma in children, for reasons other than the trauma itself (e.g. tumors of the urinary tract).


Asunto(s)
Carcinoma de Células Transicionales/diagnóstico , Neoplasias de la Vejiga Urinaria/diagnóstico , Traumatismos Abdominales/complicaciones , Adolescente , Carcinoma de Células Transicionales/complicaciones , Carcinoma de Células Transicionales/cirugía , Cistectomía , Hematuria/etiología , Humanos , Masculino , Neoplasias de la Vejiga Urinaria/complicaciones , Neoplasias de la Vejiga Urinaria/cirugía , Heridas no Penetrantes/complicaciones
11.
Int J Urol ; 12(1): 62-6, 2005 Jan.
Artículo en Inglés | MEDLINE | ID: mdl-15661055

RESUMEN

AIM: The aim of this retrospective study was to compare the results of delayed repair and early primary realignments in patients with posterior urethral injury. METHODS: From 1990 to 2003, 20 children were admitted to the Medical Faculty of Uluday University, Bursa, Turkey, for posterior urethral injuries. Traffic accidents were the most common cause of injury (n = 17). Twelve patients (60%) who were referred early (1-10 days) underwent early realignment over a urethral tube. A total of eight patients (40%) underwent delayed repair using transpubic route. In these patients, surgical repair of the urethra was performed 5-6 months later. RESULTS: Of the 12 patients who underwent early urethral realignment, six required at least one visual internal urethrotomy following the removal of the urethral catheter. Urethral stricture developed in two of 12 patients (16.6%) who underwent early urethral realignment. Of the eight patients who underwent delayed repair, six required at least one visual internal urethrotomy following removal of the urethral catheter. Urethral stricture developed in three of eight patients (37.5%) who underwent delayed repair. This difference was statistically significant (P < 0.05). CONCLUSION: The urethral stricture in patients who underwent early primary realignment was less developed than the stricture that developed in those who underwent delayed management. According to these results we recommend early primary realignment in children with posterior urethral injury.


Asunto(s)
Uretra/lesiones , Uretra/cirugía , Procedimientos Quirúrgicos Urológicos/métodos , Anastomosis Quirúrgica , Niño , Preescolar , Femenino , Humanos , Masculino , Reoperación , Estudios Retrospectivos , Factores de Tiempo , Estrechez Uretral/etiología , Estrechez Uretral/cirugía , Cateterismo Urinario , Incontinencia Urinaria/etiología
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