RESUMEN
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Asunto(s)
Humanos , Masculino , Adulto , Sarcoma de Ewing/diagnóstico por imagen , Sarcoma de Ewing/cirugía , Tumores del Estroma Gastrointestinal/diagnóstico por imagen , Hidronefrosis/diagnóstico por imagen , Diagnóstico Diferencial , Tumores del Estroma Gastrointestinal/cirugía , Inmunohistoquímica , Biopsia , Mesilato de Imatinib/administración & dosificación , Tomografía Computarizada de EmisiónAsunto(s)
Pelvis/patología , Proteína EWS de Unión a ARN/genética , Sarcoma de Ewing/diagnóstico , Sarcoma de Ewing/terapia , Abdomen/diagnóstico por imagen , Abdomen/patología , Abdomen/cirugía , Adulto , Diagnóstico Diferencial , Quimioterapia , Neoplasias Gastrointestinales/diagnóstico por imagen , Neoplasias Gastrointestinales/tratamiento farmacológico , Neoplasias Gastrointestinales/cirugía , Tumores del Estroma Gastrointestinal/diagnóstico por imagen , Tumores del Estroma Gastrointestinal/tratamiento farmacológico , Tumores del Estroma Gastrointestinal/cirugía , Humanos , Masculino , Pelvis/diagnóstico por imagen , Sarcoma de Ewing/genética , Procedimientos Quirúrgicos OperativosRESUMEN
Small cell carcinoma (SCC) of the prostate is an uncommon condition; there are very few cases in which presenting symptoms are consistent with Cushing Syndrome (CS). We report a new case in which CS triggers the suspicion of an SCC of the prostate and a review of the published cases of SCC of the prostate presenting with CS. The origin of these neoplasms is still unclear. It may be suspected when laboratory features appear in patients diagnosed with prostatic adenocarcinoma which becomes resistant to specific therapy. SCC usually occurs after the 6th decade. Patients suffering SCC of the prostate presenting with CS usually present symptoms such as hypertension, hyperglycemia, alkalosis or hypokalemia; cushingoid phenotype is less frequent. Cortisol and ACTH levels are often high. Prostatic-specific antigen levels are usually normal. CT scan is the preferred imaging test to localize the lesion, but its performance may be improved by adding other tests, such as FDG-PET scan. All patients have metastatic disease at the time of diagnosis. Lymph nodes, liver and bone are the most frequent metastases sites. Surgery and Ketokonazole are the preferred treatments for CS. The prognosis is very poor: 2- and 5-year survival rates are 27.5 and 14.3%, respectively. Key messages When a patient presents with ectopic Cushing Syndrome but lungs are normal, an atypical localization should be suspected. We should suspect a prostatic origin if Cushing Syndrome is accompanied by obstructive inferior urinary tract symptoms or in the setting of a prostatic adenocarcinoma with rapid clinical and radiological progression with relatively low PSA levels. Although no imaging test is preferred to localize these tumors, FDG-PET-TC can be very useful. Hormone marker scintigraphy (e.g. somatostatin) could be used too. As Cushing Syndrome is a paraneoplastic phenomenon, treatment of the underlying disease may help control hypercortisolism manifestations. These tumors are usually metastatic by the time of diagnosis. They have very poor prognosis.
Asunto(s)
Carcinoma de Células Pequeñas/diagnóstico por imagen , Síndrome de Cushing/etiología , Neoplasias de la Próstata/diagnóstico por imagen , Carcinoma de Células Pequeñas/complicaciones , Carcinoma de Células Pequeñas/patología , Síndrome de Cushing/diagnóstico por imagen , Humanos , Masculino , Persona de Mediana Edad , Metástasis de la Neoplasia , Tomografía de Emisión de Positrones/métodos , Pronóstico , Neoplasias de la Próstata/complicaciones , Neoplasias de la Próstata/patología , Tasa de Supervivencia , Tomografía Computarizada por Rayos X/métodosRESUMEN
Angioma serpiginosum (AS) is an unusual vascular disorder that typically affects female patients, begins in childhood and stabilizes in adulthood and not frequently involve acral skin. We herein present a 13 year-old girl with an asymptomatic erythematous punctuate first noticed on the right palm three years ago, with a proximal serpiginous progression up to the forearm. On examination there was a nonblanching erythematous punctuate on the palm and the inner aspect of right hand and forearm. Dermoscopy showed an erythematous parallel ridge pattern with some red globules and dots spreading on a linear arrangement, and the acrosyringia openings were not affected. Histopathological study showed dilated capillaries in the dermal papillae. This feature is consistent with angioma serpiginosum (AS). To the best of our knowledge, this is the first report that shows a dermoscopic image of a palmar AS. The dermoscopic pattern described in this case could aid in the diagnosis of AS and could add a value in the differential diagnosis with vascular lesions on acral skin.