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Featured researches published by Roger A. Schinella.


Journal of The American Academy of Dermatology | 1986

Eosinophilic pustular folliculitis in patients with acquired immunodeficiency syndrome: Report of three cases

Fred F. Soeprono; Roger A. Schinella

Eosinophilic pustular folliculitis is a rare disease. Highly unusual is its occurrence in three patients with acquired immunodeficiency syndrome (AIDS), described herein. This association may be the result of immunologic aberrations that are described in AIDS and may represent an abnormal reaction to skin saprophytes and dermatophytes.


The Journal of Urology | 1978

Differences in Pathological Characteristics and Prognosis of Clinical A2 Prostatic Cancer from A1 and B Disease

Mircea Golimbu; Roger A. Schinella; Pablo Morales; Shozo Kurusu

A retrospective study was done of 53 cases of clinical stages A1 to B2 prostatic carcinomas staged by pelvic lymphadenectomy. The study compared the histologic differentiation, degree of lymphocytic infiltration, incidence of lymph node metastases and type of cellular response of clinical stage A2 to stages A1 and B disease. The available data pertaining to the incidence and survival of patients with stage A2 prostatic carcinoma were analyzed. Our study indicates that 1 of every 3 unsuspected carcinomas is of clinical stage A2. The stage A2 tumors are diffused, with a higher degree of undifferentiation and a higher incidence of lymph node metastases than tumors classified clinically as stages A1 and B1. Also the survival of patients with clinical stage A2 tumors is lower than the survival of patients with clinical stage B1 disease. Clinical stage A2 tumors are more advanced biologically than clinical stage B1 tumors.


American Journal of Clinical Oncology | 2001

Megestrol and tamoxifen in patients with advanced endometrial cancer: an Eastern Cooperative Oncology Group Study (E4882).

Kishan J. Pandya; Beow Y. Yeap; Louis M. Weiner; James E. Krook; John K. Erban; Roger A. Schinella; Thomas E. Davis

To investigate the effect of adding tamoxifen to megestrol in the hormonal therapy for advanced endometrial cancer, 66 patients were entered in this study. Initially, 41 patients were randomized to either the standard progestin therapy of megestrol or to the combination of megestrol and tamoxifen between October 1982 and October 1984. The megestrol arm was terminated because of poor accrual and 25 patients were directly assigned to the combination arm. Among the 20 eligible cases on the megestrol arm, the response rate of 20% consisted of 1 complete response and 3 partial responses. The response rate on the megestrol plus tamoxifen arm was 19% with 1 (2%) complete response and 7 (17%) partial responses among 42 eligible cases. The median survival times were 12.0 months and 8.6 months, respectively. Only mild and moderate toxicities were observed on megestrol compared with more toxic complications observed on the combination of megestrol and tamoxifen, including a life-threatening case of pulmonary embolism. Although we could not carry out a comparative evaluation as intended, we conclude that the combination of megestrol and tamoxifen offers no clinical advantage over megestrol alone in the treatment of advanced endometrial carcinoma.


Human Pathology | 1985

Hermansky-Pudlak syndrome: A clinicopathologic study

Roger A. Schinella; M. Alba Greco; Stuart M. Garay; Henriette Lackner; Sandra R. Wolman; Eugene Fazzini

The Hermansky-Pudlak syndrome is a rare disease characterized by multisystemic involvement. Seven families with the disorder were identified in the Puerto Rican population of one municipal hospital, suggesting that the incidence in the Puerto Rican community is sufficient to warrant both dissemination of information about the disease and further investigation. The present study was an attempt to achieve both of these goals.


Human Pathology | 1990

Bacillary angiomatosis presenting as a soft-tissue tumor without skin involvement

Roger A. Schinella; M. Alba Greco

A patient with human immunodeficiency virus infection presented with a soft-tissue mass which histologically and clinically mimicked an angiosarcoma. Ultrastructural study, however, revealed bacteria identical to those seen in cutaneous bacillary angiomatosis, but the patient had no skin lesions. To our knowledge, this represents the first report of soft tissue involvement by bacillary angiomatosis without the presence of skin lesions.


Cancer | 1990

Lymphomatoid granulomatosis in the acquired immunodeficiency syndrome. Evidence of Epstein-Barr virus infection and B-cell clonal selection without myc rearrangement

Khushbakhat Mittal; Antonio Neri; Helen D. Feiner; Roger A. Schinella; Flores Alfonso

A case of lymphomatoid granulomatosis of lung that occurred in a patient with the acquired immunodeficiency syndrome (AIDS) was studied by light microscope, electron microscope, cell surface markers, and Southern blot test. Clonal selection of two clones of B‐cells was seen. Two clones were infected with Epstein‐Barr virus. There was no c‐myc rearrangement. Lymphomatoid granulomatosis in patients with AIDS may represent multiclonal selection of B‐lymphocytes in association with Epstein‐Barr virus infection.


Human Pathology | 1984

Fibrous hamartoma of infancy: An ultrastructural study

M. Alba Greco; Roger A. Schinella; J.C. Vuletin

The fine structures of three fibrous hamartomas of infancy were studied. All three components of these lesions were examined. The principal cells in the fibrous and myxoid areas were fibroblasts. Cells with stellate cytoplasmic projections were more prominent in myxoid areas. Myofibroblasts were abundant in two cases and not in the other. The adipose tissue component was formed by lipocytes and occasional preadipose fibroblasts. Blood vessels were more numerous in myxoid areas. Larger vessels were accompanied by smaller vessels and by clusters of cells with primitive junctions, suggesting early blood vessel formation. Some small vessels were surrounded by concentric layers of mesenchymal cells, as if attempting to form media. Electron microscopy seems to confirm the hamartomatous nature of fibrous hamartomas of infancy. The lesion appears to recapitulate the formation of blood vessels and fat, as seen in fetal tissues. Cellular myxoid areas showed prominent vasoformative proliferation, which decreased in the adipose tissue and was least prominent in the dense fibrous component. The latter may represent the end stage of the fibrous proliferation.


Diseases of The Colon & Rectum | 1977

Extragenital mixed heterologous tumor of müllerian type arising in the cecal peritoneum: Report of a case

Paul Weisz-Carrington; Bradley Bigelow; Roger A. Schinella

SummaryA mixed heterologous tumor of müllerian type arising in the cecal serosa of an elderly woman is reported. There was no history of endometriosis, and no evidence of the latter was found in the surgical specimen or at autopsy. Evidence of mesothelial origin was found microscopically in the adjacent cecal peritoneum. A review of medical literature on mixed heterologous tumors of müllerian type reveals that heretofore they have originated only in the genital system.


Urology | 1994

Carcinosarcoma of urinary bladder: report of 5 cases with immunohistologic study.

Chitra Lahoti; Roger A. Schinella; Anis F. Rangwala; Michael Lee; Howard Mizrachi

We studied 5 cases of carcinosarcoma of the urinary bladder. Immunoperoxidase studies were performed to identify the nature of the tumor and to establish the diagnosis. We suggest that these tumors represent a transition of epithelial to mesenchymal malignancy. Three of our patients had a history of radiation therapy prior to development of carcinosarcoma; of which 2 had a long interval between exposure to radiation and tumor development. Radiation is a risk factor for endometrial carcinosarcoma, and in this report we strongly suggest such an association for the urinary bladder.


Urology | 1974

Posthitis xerotica obliterans in circumcision specimens

Roger A. Schinella; Dairton Miranda

Abstract Histologic examination of foreskins submitted from circumcisions in patients with phimosis revealed 22 cases of posthitis xerotica obliterans from 1956 to mid-1973. From 1970 to 1973 a tabulation of all specimens showed the exact incidence of this entity to be 3.6 per cent. Fifteen of 22 cases found were in children less than thirteen years of age, the youngest being four years. There was a correlation of the histologic severity of the changes of posthitis xerotica obliterans with the severity of clinical symptoms. A 32 per cent incidence of urinary obstructive changes was noted.

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Sandra R. Wolman

George Washington University

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Arthur S. Patchefsky

Thomas Jefferson University Hospital

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Charles A. Sklar

Memorial Sloan Kettering Cancer Center

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