[Pheochcromocytoma, report of 10 cases]

The pheochromocytoma is a rare endocrine tumor, issued from the chromaffine surrenalian or extra-surrenalian tissue. We report a retrospective study of 10 cases of pheochromocytoma collected during a period 3 years. Our study concerned 3 men and 7 women, with an average age of 32, 5 years. Revealing symptomatology was dominated by an arterial hypertension [8 cases]. The triad of Menard [headaches, sweating and palpitations] was found in 6 cases. The biological assessment found a rise in the urinary catecholamine. Complementary exams [ultrasonography, tomodensitometry, magnetic resonances] were usefull for the location of the tumor. The adenalectomy realised by transperitoneal under costal way was realised in all the cases. Histological examination confirmed the diagnosis. The pheochromocytoma is a neuroendocrine tumor of neuroectodermic origin. The clinical and biological presentations depend on the importance of the hypersecretion of catecholamines. The treatment is surgical. The objective of this study is to insist on the rarity of this pathology, the diagnostic difficulties, the severity of this pathology and curability of the benign forms

Renal hydatid cyst: Retrospective analysis of 15 cases

To analyze of the various epidemiological, clinical and therapeutical aspects of renal hydatid cyst. In this retrospective study we evaluated 15 cases of renal hydatid cysts treated at the Urology Department of Ibn Rochd University Hospital, Casablanca, between January 2004 and December 2007. The patient group consisted of 7 men and 8 women with a mean age of 40 [range 23-70] years. The parameters studied included the presenting symptoms, the findings on clinical and radiological investigations and the methods of treatment. The patients presented within a mean period of 14 months from the onset of symptoms. Presenting symptoms included pain, hydaturia, hematuria and the presence of a tumoral mass on palpation. Intravenous urography [IVU] revealed calcifications in one patient, a mass lesion in two patients and a non-functioning kidney in one patient. A CT scan of the abdomen was carried out in 6 patients where the radiological examination was inconclusive. However, all patients were subjected to ultrasonography, which remains the diagnostic modality of choice. Hydatid serology was positive in 8 patients. Treatment consisted of unroofing of the cyst in 13 patients and pericystectomy and nephrectomy in one patient each. During the post-operative period 2 patients developed urinary fistulae. After a follow-up of 30 months all patients are symptom-free. In the Maghreb region, where hydatidosis is endemic, the kidneys are rarely affected. The diagnosis of renal hydatid cysts mainly depends on sonography. CT scan is useful in cases with doubtful diagnosis. Magnetic resonance imaging [MRI] is the modality of choice in cases with atypical forms and helps in differentiating a renal hydatid cyst from a serous cyst or cystic renal cancer

new case of intrascrotal cystic lymphangioma

Cystic lymphangioma of the scrotum is a rare benign tumor of the lymphatic system with very few cases described in the literature. We report the case of a 23-year-old patient admitted to our service with the presumptive diagnosis of a right-sided hydrocele. Surgical exploration revealed a moderately sized multi-septated hydrocele, chronic inflammation and thickening of the tunica vaginalis and a small cystic mass 1 cm in size near the head of the epididymis, but separate from it, the testis and the spermatic cord. Treatment consisted of surgical excision of the mass and resection of the tunica vaginalis. Histological examination revealed a cystic lymphangioma. The objective of this article is to report the clinical presentation, diagnostic and therapeutic aspects of scrotal cystic lymphangiomas