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Biomedical subjects

O G Solis

Publications and source records attributed to O G Solis.

7 recordsLinked to original sources
PubMed1993

Primary gastric adenosarcoma.

We describe the first case, to our knowledge, of a primary gastric adenosarcoma surgically resected from a 46-year-old white man. This biphasic neoplasm, well described in the female genital tract, was composed of cytologically benign tubular and cystic glands widely dispersed within a sarcomatous stromal component. Immunohistochemically, the epithelial elements were positive for cytokeratin, while the stromal elements were positive for vimentin and desmin. The clinical and pathologic features of pelvic adenosarcomas are described and compared with the tumor of the stomach. Although accurate prediction of the biologic behavior of this gastric neoplasm is difficult, the high mitotic rate in the sarcomatous component and the infiltration of the gastric serosal surface by the tumor were considered to be ominous prognostic features.

Humans↗
PubMed1992

DNA ploidy of oncocytic-granular renal cell carcinomas and renal oncocytomas by image analysis.

DNA ploidy analysis of five renal oncocytomas, six pure oncocytic-granular renal cell carcinomas, 15 pure clear cell renal carcinomas, and two cases of mixed oncocytic-granular and clear cell heterogenous renal cell carcinomas were determined on Feulgen-stained paraffin sections using the (CAS-200 image Analyzer). All five renal oncocytomas were diploid, as were six oncocytic-granular renal cell carcinomas. Three of the 15 clear renal cell carcinomas were aneuploid. In one heterogeneous renal cell carcinoma, the oncocytic-granular foci were diploid and the clear cell focus was aneuploid. The other heterogeneous renal cell carcinoma was uniformly diploid. In 21 renal cell carcinomas, one of 14 stage I tumors was aneuploid, all four stages II and III tumors were diploid, and two of three stage IV cases were aneuploid. All stages I, II, and III patients were free of disease 3 to 48 months after surgery. All three stage IV cases were dead of their disease within 36 months of surgery. We conclude that DNA analysis by image cytometry best identifies the heterogeneity of ploidy patterns in mixed cell type carcinomas, generally correlates with the stage of disease, and may be of value in predicting overall prognosis of renal epithelial neoplasms. DNA analysis by image cytometry, however, did not reveal significant differences between oncocytic granular cell carcinoma and oncocytoma, since both lesions were generally diploid. The distinction between the two tumors is best made on morphologic grounds.

Adenoma↗
PubMed1991

Extragenital primary mixed malignant mesodermal tumor.

Malignant mixed mesodermal tumors (MMMT) are infrequent neoplasms characteristically arising in the endometrium. Extragenital MMMTs are extremely rare, with but 11 cases reported in the literature. Previous extragenital MMMTs have been associated with endometriosis, Wolfian duct remnants, and ovarian cyst adenocarcinoma and have been presumed to arise from coelomic and subcoelomic structures. We report a case of a MMMT arising extragenitally in the cul-de-sac in a 54-year-old White female patient in whom disseminated intraperitoneal serosal papillary serous adenocarcinoma of the peritoneum was present. The histogenesis of this rare neoplasm is discussed along with a brief review of previously reported cases.

Carcinoma, Squamous Cell↗
PubMed1986

Pseudogaucher cells in Mycobacterium avium intracellulare infections in acquired immune deficiency syndrome (AIDS).

This report describes a 28-year-old woman with the acquired immune deficiency syndrome (AIDS) with culture-proven disseminated Mycobacterium avium intracellulare infection. The histopathologic and cytologic features in this case were unique in that these organisms that stained positively with the Ziehl-Neelsen and periodic acid-Schiff (PAS) stains were numerous, present intracellularly within histiocytes, transforming them into pseudogaucher cells. Differential diagnostic criteria for pseudogaucher cells and abnormal macrophage handling of the intracellular organisms in AIDS are discussed.

Acquired Immunodeficiency Syndrome↗