A case of tubulocystic carcinoma of the kidney with aggressive features

Tubulocystic carcinoma of the kidney is rare and typically indolent. Our case involved an aggressive tubulocystic carcinoma as well as the radiological confirmation of its relation to papillary renal cell carcinoma. A 46-year-old male presented with renal multiloculated cysts with a solid part. On computed tomography and magnetic resonance imaging, the solid part showed the characteristics of papillary renal cell carcinoma. Contrast enhancement of the solid part was fluffy and sparse because of the coexistence of cysts. Perirenal fat invasion resulted in exophytic cysts, and renal-hilar cystic lymph node metastasis existed. The histopathological diagnosis was tubulocystic carcinoma associated with areas of papillary renal cell carcinoma and poorly differentiated carcinoma with metastasis. Our case suggests that the solid part enhancement of tubulocystic carcinoma tends to be fluffy and sparse, and exophytic cysts and cystic lymph nodes may show radiologically aggressive findings.     

A study of the relationship between a self-report measure and a behavioral measure of impulsive behavior

The measures used in previous studies did not consider the situation where an individual exhibits impulsive behavior. The present research examines the relationship between self-reported measures and behavioral measures of impulsive abandonment and panic behavior in a problem-solving situation. The self Impulsive Behavior Questionnaire was the self-reported measure of the impulsive behavior tendency. The 91 undergraduate participants were grouped based on this score (high, n = 31; middle, n = 33; low, n = 27) were used. The behavioral measures were the correct detection and commission errors on the Continuous Performance Test. The result showed that the high impulsive group made a significantly higher number of commission errors than did the low group. The findings of this study support a consistent relationship between behavioral and self-reported measures.     

Malignant solitary fibrous tumor of the soft tissue: a cytogenetic study

We report on a case of a solitary fibrous tumor that developed in the thigh of an 82-year-old woman. The tumor was composed of areas of high-grade sarcoma and typical solitary fibrous tumor. Its karyotype was: 70,XXX,+X[4],+1[2],add(1)(p36)[4],add(1)[2],+2[4],-3[4],+6[4],add(6)(p11)x2[4],+7[4],+9[3],-11[4],-12[4],-13[4],add(13)(p11)x2[4],-14[4],+15[4],-16[3],-17[4],-19[4],+20,[4],+21[4],+22[2],+mar1x2[4][cp4].