Pleomorphic hyalinizing angiectatic tumor of the male breast: a heretofore unreported occurrence.

Pleomorphic hyalinizing angiectatic tumor (PHAT) is considered an unusual mesenchymal tumor of intermediate malignant potential that is distinguished by a prominent angiectatic vasculature with clusters of thin-walled, fibrin-lined vessels surrounded by sheets of spindled and pleomorphic cells. This lesion occurs mostly in the subcutaneous soft tissues of the lower extremities. In this paper, the authors report the first case of PHAT involving the breast parenchyma of a 75-year-old man.

Large cell neuroendocrine carcinoma of the lung: a 10-year clinicopathologic retrospective study.

Background: Large cell neuroendocrine carcinoma is a recently recognized histologic entity whose clinical features and optimal treatment have not yet been well defined and are still being assessed. We report our retrospective assessment of cases of large cell neuroendocrine carcinoma observed from 1989 to 1999 in terms of survival.

Methods: Cases of large cell neuroendocrine carcinoma diagnosed between 1989 and 1999 were reassessed retrospectively according to the World Health Organization classification.

Solitary fibrous tumor of the spinal nerve rootlet: report of a case mimicking schwannoma.

We report a case of solitary fibrous tumor involving the spinal nerve root at the L1-L2 level in a 67-year-old man. The patient presented with lumbar pain and weakness in his right lower extremity. Histologically, the tumor was composed of a proliferation of monomorphous spindle cells in an abundant collagenous stroma; neither necrosis nor mitoses were evident.

[Mixed neoplasia of the stomach: description of a case of tubular adenoma combined with carcinoid].

We report about a gastric polyp that was a combination of tubular adenoma and carcinoid. The patient, a 76 year-old male, presented with 1 cm sessile polyp, located in the gastric body, that was a combination of a tubular adenoma with moderate dysplasia and a small carcinoid. Immunohistochemically, the latter component was positive for chromogranin and synaptophysin.

[Enterocolic phlebitis. Description of a case and review of the literature].

Objective: To report about a case of enterocolic phlebitis, a rare cause of ischemic intestinal necrosis.

Results And Conclusions: The patient, a 71 year-old male, presented with signs of acute abdomen. A right hemicolectomy was performed, which revealed a tubulovillous adenoma with high grade dysplasia located in the ascending colon, and a diffuse ischemic colitis.