ABSTRACT
OBJECTIVE: We report one case of a spontaneous resolution of a uretero-vaginal fistula, and we review the current diagnostic and therapeutic features of this condition in the literature. METHODS: We present the case of a 41-year-old woman who, during the late postoperative period of a radical hysterectomy, presented episodes of daily and nocturnal incontinence with episodic flank pain compatible with uretero-vaginal fistula. RESULTS: One month after diagnosis the patient does not report incontinence during day or night, and the lumbar pain has disappeared. An intravenous urography shows that there has been a spontaneous resolution of the uretero-vaginal fistula. CONCLUSIONS: Spontaneous resolution of a uretero-vaginal fistula is rare. Most fistulas require endourological or surgical treatment.
Subject(s)
Ureteral Diseases/pathology , Vaginal Fistula/pathology , Adult , Female , Humans , Hysterectomy , Magnetic Resonance Imaging , Male , Postoperative Complications/pathology , Ureteral Diseases/complications , Urinary Fistula/pathology , Urinary Fistula/surgery , Urinary Incontinence/etiology , Urography , Vaginal Fistula/complicationsABSTRACT
OBJETIVO: Presentar un caso de corrección espontánea de fístula urétero-vaginal y revisar aspectos diagnósticos y terapéuticos de la literatura actual.MÉTODO: Presentamos el caso de una mujer de 41 años que en el postoperatorio tardío de una histerectomía radical inicia un cuadro de episodios de incontinencia diurna y nocturna leves con dolor episódico en el flanco derecho compatibles con fístula urétero-vaginal. RESULTADOS: Pasado un més del diagnóstico la paciente no refiere incontinencia diurna ni nocturna y el dolor lumbar ha desaparecido. Se comprueba mediante urografía intravenosa corrección espontánea de la fístula urétero-vaginal.CONCLUSIONES: La resolución espontánea de la fístula urétero-vaginal es infrecuente. La mayoría de las fístulas requieren tratamiento endourológico o quirúrgico(AU)
OBJECTIVE: We report one case of a spontaneous resolution of a uretero-vaginal fistula, and we review the current diagnostic and therapeutic features of this condition in the literature.METHODS: We present the case of a 41-year-old woman who, during the late postoperative period of a radical hysterectomy, presented episodes of daily and nocturnal incontinence with episodic flank pain compatible with uretero-vaginal fistula.RESULTS: One month after diagnosis the patient does not report incontinence during day or night, and the lumbar pain has disappeared. An intravenous urography shows that there has been a spontaneous resolution of the uretero-vaginal fistula.CONCLUSIONS: Spontaneous resolution of a uretero-vaginal fistula is rare. Most fistulas require endourological or surgical treatment(AU)
Subject(s)
Humans , Female , Adult , Vesicovaginal Fistula/diagnosis , Vesicovaginal Fistula/surgery , Vesicovaginal Fistula/urine , Urinary Incontinence/complications , Urinary Incontinence/diagnosis , Urinary Incontinence/pathology , Urography/methods , Urography , Postoperative Complications , Hysterectomy/instrumentation , Hysterectomy/methods , Hysterectomy , Catheterization/methods , Catheterization , Postoperative Complications/therapyABSTRACT
OBJECTIVE: We present the case of a big retroperitoneal tumor that received the pathologic diagnosis of malignant fibrous histiocytoma. We also review the diagnostic and therapeutic features of this disease in the current literature. METHODS: We present the case of a 75-year-old male who was admitted to the Gastrointestinal Disease Department with asthenia of several months of evolution and gastrointestinal problems. Abdominopelvic CT scan revealed a big mass of 20 x 22 x 12 cm, which seems to depend from the left kidney, together with an 8 cm diameter abdominal aortic aneurysm. RESULTS: The patient underwent surgery and left radical nephrectomy together with radical resection of the retroperitoneal mass were performed. Pathology reportes malignant fibrous histiocytoma of the storiform-pleomorphic type, with hyaline degeneration foci (stadium pT2B). CONCLUSIONS: Sarcomas are rare neoplasias. They can adopt several different morphologic patterns, as well as many differentiation degrees. The surgical treatment is still the only therapy with healing possibilities. Adjuvant treatments through radiotherapy and/or chemotherapy are brought into question.
Subject(s)
Histiocytoma, Malignant Fibrous , Retroperitoneal Neoplasms , Aged , Histiocytoma, Malignant Fibrous/diagnosis , Humans , Male , Retroperitoneal Neoplasms/diagnosisABSTRACT
OBJETIVO: Presentar un caso de una tumoración retroperitoneal de gran tamaño con diagnóstico patológico de Histiocitoma fibroso maligno y revisar aspectos diagnósticos y terapéuticos de la literatura actual.MÉTODO: Presentamos el caso de un hombre de 75 años de edad que durante un ingreso en el servicio de digestivo por clínica de astenia de meses de evolución y problemas gastrointestinales se realiza CT abdomino-pélvico, identificando gran masa de 20 x 22 x 12 cm que parece depender del riñón izquierdo junto a aneurisma de aorta abdominal de 8 cm de diámetro.RESULTADOS: Se somete al paciente a intervención quirúrgica donde se realiza Nefrectomía radical izquierda más resección radical de masa retroperitoneal, que histológicamente corresponde a un Histiocitoma fibroso maligno, tipo estoriforme-pleomórfico con focos de degeneración hialina (Estadio pT2b).CONCLUSIONES: Los sarcomas son neoplasias infrecuentes. Pueden adoptar una gran variedad de patrones morfológicos y distintos grados de diferenciación. El tratamiento quirúrgico continúa siendo la única terapia con posibilidades curativas. El tratamiento adyuvante radioterápico y/o quimioterápico es cuestionado (AU)
OBJECTIVE: We present the case of a big retroperitoneal tumor that received the pathologic diagnosis of malignant fibrous histiocytoma. We also review the diagnostic and therapeutic features of this disease in the current literature.METHODS: We present the case of a 75-year-old male who was admitted to the Gastrointestinal Disease Department with asthenia of several months of evolution and gastrointestinal problems. Abdominopelvic CT scan revealed a big mass of 20 x 22 x 12 cm, which seems to depend from the left kidney, together with an 8 cm diameter abdominal aortic aneurysm.RESULTS: The patient underwent surgery and left radical nephrectomy together with radical resection of the retroperitoneal mass were performed. Pathology reportes malignant fibrous histiocytoma of the storiform-pleomorphic type, with hyaline degeneration foci (stadium pT2B).CONCLUSIONS: Sarcomas are rare neoplasias. They can adopt several different morphologic patterns, as well as many differentiation degrees. The surgical treatment is still the only therapy with healing possibilities. Adjuvant treatments through radiotherapy and/or chemotherapy are brought into question (AU)
Subject(s)
Humans , Male , Aged , Histiocytoma, Malignant Fibrous/diagnosis , Histiocytoma, Malignant Fibrous/pathology , Histiocytoma, Malignant Fibrous/surgery , Retroperitoneal Neoplasms/diagnosis , Retroperitoneal Neoplasms/surgery , Tomography/methods , Tomography , Nephrectomy/methods , NephrectomySubject(s)
Nephrectomy , Polycystic Kidney Diseases/surgery , Humans , Kidney Transplantation , Male , Middle Aged , Preoperative CareSubject(s)
Humans , Male , Aged, 80 and over , Cysts/diagnosis , Kidney Neoplasms/diagnosis , Abdomen, Acute/etiology , Diagnosis, DifferentialSubject(s)
Humans , Male , Middle Aged , Polycystic Kidney Diseases/surgery , Nephrectomy , Kidney TransplantationABSTRACT
OBJECTIVE: We report a rare case of malignant priapism secondary to transitional cell carcinoma. METHODS: The patient with bladder cancer (pT4G3) presented with painful penile erection. Corpora cavernosa biopsy was done. RESULTS: The pathologic diagnosis was penile metastasis of transitional cell carcinoma. CONCLUSIONS: Priapism secondary to penile metastasis of transitional cell carcinoma is rare and indicates advanced disease with a poor prognosis.
Subject(s)
Carcinoma, Transitional Cell/complications , Priapism/etiology , Urinary Bladder Neoplasms/complications , Humans , MaleABSTRACT
OBJETIVO: Presentamos un caso infrecuente de priapismo maligno secundario a carcinoma de celulas transicionales de la vejiga.MÉTODOS: El paciente portador de un cancer vesical (pT4G3) presenta una tumefacción dolorosa peneana. Realizamos biopsia de los cuerpos cavernosos.RESULTADOS: El informe de la anatomía patológica muestra metástasis peneana de carcinoma de células de transición.CONCLUSIONES: El priapismo secundario a metástasis peneana por carcinoma transicional es infrecuente y se asocia a un mal pronóstico debido a que su presencia indica diseminación metastática multiorgánica(AU)
OBJECTIVE: We report a rare case of malig-nant priapism secondary to transitional cell carcinoma.METHODS: The patient with bladder cancer (pT4G3) pre-sented with painful penile erection. Corpora cavernosa biopsy was done.RESULTS: The pathologic diagnosis was penile metastasis of transitional cell carcinoma.CONCLUSIONS: Priapism secondary to penile metastasis of transitional cell carcinoma is rare and indicates advanced disease with a poor prognosis(AU)