100,345 research outputs found
Testicular cystic dysplasia: evaluation of 3 new cases treated without surgery
PURPOSE: We describe 3 cases of testicular cystic dysplasia that were diagnosed only by sonography to avoid an invasive approach.
MATERIALS AND METHODS: Three patients 5, 8 and 12 years old, respectively, had increased testicular volume and/or intermittent pain. Sonographic examination of the testis by high frequency (7.5 mHz.) probes showed the typical onset of testicular cystic dysplasia, characterized by several small focal or diffuse intraparenchymal cystic formations.
RESULTS: Biopsy or orchiectomy was not considered. At 16, 18 and 24 months of followup, respectively, testicular pain was absent in our 3 cases and sonographic findings were unchanged.
CONCLUSIONS: Clinical and sonographic followup is considered sufficient to evaluate possible changes in the clinical course of this pathological condition which, although benign, still remains to be defined
CT analysis of ovarian tumors: Correlations with laparoscopical and surgical findings
This study concerns a selected group of 21 patients with ovarian carcinoma in whom CT, laparotomy, and laparoscopy findings could be compared. Considering the loco-regional and distant abdominal sites of involvement, the limits and possibilities of CT in diagnosis and follow-up are outline
Letter, [Author unclear] to Paulina T. Merritt
Handwritten letter to Paulina Merritt from an unknown author, October 1, 1876.
Radiological assessment of paediatric fungal infections: A pictorial review with focus on PET/MRI
Multiple synchronous tumors in a child with Fanconi anemia
Fanconi anemia (FA) is an autosomal recessive inherited syndrome characterized by congenital abnormalities, aplastic anemia, and a high likelihood of developing cancer. We describe a child who presented with 2 synchronous solid tumors (Wilms tumor and neuroblastoma), later found to have FA, who developed severe toxicity and died after a first cycle of chemotherapy. Our experience emphasizes that a predisposing genetic condition should be sought in cases of multiple tumors and that managing FA patients with cancer can be particularly difficul
Multifocal hepatoblastoma: is there a place for partial hepatectomy?
Proceedings of the Tumor Board of the
Hematology–Oncology Division of the Department of
Pediatrics, University of Padua, Padua, Ital
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