Publications by authors named "Rafael Padilla Longoria"

Article Synopsis
  • Hepatocellular adenomas (HCA) are uncommon and non-cancerous tumors that form from liver cells, and recent advances have enhanced our understanding of them.
  • The article discusses a notable case of a 20-year-old patient with a large inflammatory HCA, who underwent surgery to remove part of the liver.
  • After a smooth three-day recovery in the hospital, follow-up tests at eight months showed no signs of the tumor returning.
View Article and Find Full Text PDF

We present a case report of a giant solitary fibrous tumor (SFT) with a review of the literature and discuss its biological features and diagnosis. A 43-year-old man presented to our emergency department with abdominal pain and distension with an evolution of two days. Contrast-enhanced computed tomography (CT) showed a large, well-circumscribed semisolid mass (12 cm x 10 cm x 12 cm) localized in the pancreatic head.

View Article and Find Full Text PDF

A literature review on desmoid tumors was carried out, which are tumors that affect soft tissues with a locally aggressive behavior and are unable to metastasize. Sporadic cases are located on the extremities and chest wall; hereditary cases have an intra-abdominal predilection, and those associated with pregnancy occur on the abdominal wall. Imaging techniques assess disease extension.

View Article and Find Full Text PDF

Struma ovarii is a rare monodermal variant of ovarian teratoma that contains at least 50% thyroid tissue. Less than 8% of struma ovarii cases present with clinical and biochemical evidence of thyrotoxicosis due to ectopic production of thyroid hormone and only 5% undergo malignant transformation into a papillary thyroid carcinoma. Only isolated cases of hormonally active papillary thyroid carcinoma developing within a struma ovarii have been reported in the literature.

View Article and Find Full Text PDF

Background: Neuroblastoma is a common malignancy in infancy but extremely rare in adults. These tumors, commonly found in the abdomen, originate in the sympathetic nervous system. Staging and management are standardized in children and adults, although their prognosis is very different, being more aggressive and with a poorer outcome in the adult.

View Article and Find Full Text PDF

Adamantinomas are rare, low-grade malignant intra-osseous tumors composed of epithelial and mesenchymal elements, which show a marked predilection for the tibia and fibula of young adult male patients. Although cases of adamantinoma located to the axial skeleton have been reported either as recurrent or metastatic disease, only two cases of primary adamantinoma located to the thoracic wall have been previously described. In this study we present the clinical, radiological and histopathological features of a 24-year-old male with a slow growing, solid-cystic, painful mass, located to the right 11th rib, which was morphological and immunohistochemically diagnosed as a primary classic adamantinoma.

View Article and Find Full Text PDF

Objectives: To analyze presentation, diagnosis and treatment of islet cell tumors at the ABC Medical Center.

Materials And Methods: Medical records of the 7 patients with endocrine tumors diagnosed between 1995 and 2005 were reviewed and analyzed, with emphasis to clinical, biochemical and radiological characteristics, surgical treatment and outcome.

Results: There were 3 insulinomas, 1 gastrinoma, 1 VIPoma, and 2 non-functioning tumors.

View Article and Find Full Text PDF