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1.
Cureus ; 15(8): e42929, 2023 Aug.
Artículo en Inglés | MEDLINE | ID: mdl-37667725

RESUMEN

Xanthogranulomatous pyelonephritis (XGP) is an uncommon condition representing 1% of all renal infections. XGP due to complicated pyelonephritis associated with hepatic abscess is an extremely rare complication and has rarely been reported in the literature. We report a rare case of a 54-year-old female with a history of diabetes and recurrent urinary tract infections (UTI) who presented with acute right flank pain and fever which had been ongoing for four days. CT scan showed multiple bilateral obstructive nephrolithiasis associated with a liver abscess. Given the patient's high risk of nephron loss, a bilateral renal and liver abscess drainage followed by a two-stage flexible ureterorenoscopy (FURS) was performed. One week later, a CT scan showed a typical radiological aspect of XGP on the right kidney invading the liver. She urgently underwent a right nephrectomy with an uneventful outcome. In conclusion, the diagnosis of XGP should be considered in the presence of complicated pyelonephritis associated with hepatic abscess.

2.
Pan Afr Med J ; 43: 56, 2022.
Artículo en Inglés | MEDLINE | ID: mdl-36578814

RESUMEN

Leiomyosarcoma of the prostate is an extremely rare neoplasm. It represents less than 0.1% of all prostate malignancies. It is considered to have a poor prognosis, an aggressive nature, and high metastatic potential. Additionally, the relationship between radiation exposure for the treatment of primary prostatic cancer and the occurrence of leiomyosarcoma as second cancer at the irradiated site is rare, with unknown etiology. We reported a 72-year-old male known case of prostate adenocarcinoma with radio-hormonotherapy for six years who presented with acute urinary retention. Magnetic resonance imaging revealed a large malignant obstructive prostate with direct invasion of surrounding organs and multiple metastases. Trans-urethral resection of the prostate was performed, and the histopathology result showed high-grade leiomyosarcoma. The patient passed away after four months due to multiorgan failure. In conclusion, there may be a causal relationship between radiation therapy to the prostate and the development of prostate leiomyosarcoma.


Asunto(s)
Leiomiosarcoma , Hiperplasia Prostática , Neoplasias de la Próstata , Masculino , Humanos , Anciano , Próstata/patología , Leiomiosarcoma/diagnóstico , Leiomiosarcoma/etiología , Leiomiosarcoma/radioterapia , Neoplasias de la Próstata/patología
3.
Pan Afr Med J ; 43: 136, 2022.
Artículo en Inglés | MEDLINE | ID: mdl-36762167

RESUMEN

Penile calciphylaxis is a rare and highly morbid condition mainly affecting diabetic patients with chronic renal failure (CRF). It is characterized by ischemic skin ulceration and necrosis secondary to dystrophic calcification of the subcutaneous penile tissue and penile arterioles. We report a 52-year-old male with a 6-year history of diabetes mellitus and CRF on hemodialysis, who presented with a painful penile necrotic lesion in the last three weeks. He firstly treated with medical treatment, which was failed. Then underwent total penectomy. The histopathology result confirmed the diagnosis of penile calciphylaxis. Unfortunately, he passed away due to septic shock and multisystem organ failure ten days after surgery. In conclusion, the diagnosis of penile calciphylaxis must be evoked in the presence of any minimal necrotic penile lesion in a patient with CRF; this will initiate quick medical and/or minimally invasive surgical treatment to improve the patient's prognosis and avoid serious complications.


Asunto(s)
Calcifilaxia , Fallo Renal Crónico , Enfermedades del Pene , Masculino , Humanos , Persona de Mediana Edad , Calcifilaxia/diagnóstico , Calcifilaxia/etiología , Calcifilaxia/terapia , Enfermedades del Pene/diagnóstico , Enfermedades del Pene/etiología , Enfermedades del Pene/patología , Fallo Renal Crónico/complicaciones , Fallo Renal Crónico/terapia , Diálisis Renal/efectos adversos , Pene , Necrosis/patología
5.
Can Urol Assoc J ; 8(3-4): E207-9, 2014.
Artículo en Inglés | MEDLINE | ID: mdl-24678368

RESUMEN

The renocolic fistula is a rare entity. We report 2 cases of renocolic fistula penetrating an abdominal trauma from a gunshot.

6.
Scand J Urol Nephrol ; 37(2): 179-80, 2003.
Artículo en Inglés | MEDLINE | ID: mdl-12745730

RESUMEN

Paratesticular adenofibroma is an uncommon benign tumour. Although it has previously been reported in the female reproductive organs, to our knowledge only three cases have previously been reported in the male genital organs. Herein we describe an adenofibroma that developed in the tunica vaginalis and rete testis. We discuss its histogenesis and conservative treatment.


Asunto(s)
Adenofibroma/patología , Neoplasias Testiculares/patología , Adulto , Diagnóstico Diferencial , Humanos , Masculino
7.
Scand J Urol Nephrol ; 37(2): 189-90, 2003.
Artículo en Inglés | MEDLINE | ID: mdl-12745734

RESUMEN

Hypercalcaemia is a frequent complication of multiple myeloma. A mild degree of nephrocalcinosis has been noted in occasional patients and renal calculi are also sometimes present. We report herein a case of multiple myeloma that was revealed by the presence of bilateral calcium renal staghorn calculi. Medical treatment of myeloma, surgical management of this complex lithiasis and the course of multiple myeloma are discussed.


Asunto(s)
Cálculos Renales/etiología , Mieloma Múltiple/diagnóstico , Diagnóstico Diferencial , Femenino , Humanos , Cálculos Renales/diagnóstico por imagen , Persona de Mediana Edad , Mieloma Múltiple/complicaciones , Mieloma Múltiple/terapia , Nefrostomía Percutánea , Radiografía
8.
Prog Urol ; 12(3): 459-61, 2002 Jun.
Artículo en Francés | MEDLINE | ID: mdl-12189755

RESUMEN

Non-secreting malignant adrenal cortical adenoma is rare and the bilateral form is exceptional. Diagnosis is often delayed and it has a very poor prognosis. The authors report a case of bilateral adrenal cortical adenoma in a 53-year-old man.


Asunto(s)
Neoplasias de la Corteza Suprarrenal/diagnóstico , Adenoma Corticosuprarrenal/diagnóstico , Neoplasias Primarias Múltiples/diagnóstico , Neoplasias de la Corteza Suprarrenal/cirugía , Adenoma Corticosuprarrenal/cirugía , Resultado Fatal , Humanos , Masculino , Persona de Mediana Edad , Neoplasias Primarias Múltiples/cirugía
9.
Prog Urol ; 12(1): 105-7, 2002 Feb.
Artículo en Francés | MEDLINE | ID: mdl-11980001

RESUMEN

The authors report a case of a 30-year-old patient presenting with a right testicular mass. The presumptive diagnosis was that of a malignant tumour. The definitive diagnosis, confirmed by histological examination of the orchidectomy specimen, was that of a dermoid cyst. The aetiopathogenic, diagnostic and therapeutic characteristics of this exceptional disease are reported.


Asunto(s)
Quiste Dermoide/diagnóstico , Neoplasias Testiculares/diagnóstico , Adulto , Quiste Dermoide/cirugía , Humanos , Masculino , Neoplasias Testiculares/cirugía
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