Search Results - "Rabkin, Michael S"

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    The utility of cytokeratin 5/6 in the recognition of cutaneous spindle cell squamous cell carcinoma by Sigel, Jessica E., Skacel, Marek, Bergfeld, Wilma F., House, Nancy S., Rabkin, Michael S., Goldblum, John R.

    Published in Journal of cutaneous pathology (01-11-2001)
    “…Background: Cutaneous spindle cell squamous cell carcinoma (SSCC) is a challenging diagnosis since it may be difficult to distinguish from spindle cell…”
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    Granular cell variant of epithelioid cell histiocytoma by Rabkin, Michael S, Vukmer, Tyler

    Published in The American journal of dermatopathology (01-10-2012)
    “…Classic granular cell tumors (GCTs) stain strongly and uniformly positive for S100 protein and are believed to show Schwann cell derivation. Polypoid cutaneous…”
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    The limited specificity of histological examination in the diagnosis of dysplastic nevi by Rabkin, Michael S.

    Published in Journal of cutaneous pathology (01-11-2008)
    “…Dysplastic nevi were originally described as a distinct entity with specific clinical and histological features of importance as direct precursors of malignant…”
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    Multiple Hybrid Granular Cell Tumor-Perineuriomas by ZARINEH, Alireza, COSTA, Melanie E, RABKIN, Michael S

    Published in The American journal of surgical pathology (01-10-2008)
    “…Hybrid peripheral nerve sheath tumors (PNSTs) are recently recognized, rarely reported entities. Very few hybrid PNSTs with elements of perineurioma have been…”
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    Clinicopathologic, immunophenotypic, and molecular cytogenetic fluorescence in situ hybridization analysis of primary and secondary cutaneous follicular lymphomas by KIM, Bong K, SURTI, Urvashi, PANDYA, Amit, COHEN, Jack, RABKIN, Michael S, SWERDLOW, Steven H

    “…Although primary cutaneous follicular lymphoma (FL) is considered a distinct variant of FL in the World Health Organization classification ("cutaneous follicle…”
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    Atypical spitz nevi/tumors: Lack of consensus for diagnosis, discrimination from melanoma, and prediction of outcome by Barnhill, Raymond L, Argenyi, Zsolt B, From, Lynn, Glass, L.Frank, Maize, John C, Mihm, Martin C, Rabkin, Michael S, Ronan, Salve G, White, Wain L, Piepkorn, Michael

    Published in Human pathology (01-05-1999)
    “…The biological nature of Spitz nevi/tumors and their diagnostic distinction from, or relationship to, melanoma remain unresolved issues. In this report, a…”
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    Smooth muscle hamartoma associated with a congenital pattern melanocytic nevus, a case report and review of the literature by Zarineh, Alireza, Kozovska, Milena E., Brown, William G., Elder, David E., Rabkin, Michael S.

    Published in Journal of cutaneous pathology (01-10-2008)
    “…Smooth muscle hamartoma (SMH) is a rare benign congenital or acquired lesion sometimes associated with Becker’s nevus (Becker’s melanosis). We report an…”
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    Analysis of therapeutic and immunologic effects of R24 anti‐GD3 monoclonal antibody in 37 patients with metastatic melanoma by Kirkwood, John M., Mascari, Ruth A., Edington, Howard D., Rabkin, Michael S., Day, Roger S., Whiteside, Theresa L., Vlock, Daniel R., Shipe‐Spotloe, Janice M.

    Published in Cancer (15-06-2000)
    “…BACKGROUND Antitumor effects of antibodies against ganglioside antigens of melanoma have been reported, but neither optimal doses nor mechanisms have been…”
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    Mohs Micrographic Surgery for the Eradication of Phaeohyphomycosis of the Hand by Bogle, Melissa A., Rabkin, Michael S., Joseph, Aaron K.

    Published in Dermatologic surgery (01-02-2004)
    “…Background. PHAEOHYPHOMYCOSIS is a rare mycotic infection that is caused by dematiaceous fungi requiring surgical excision or long‐term use of oral antifungal…”
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    Histological characteristics of metastasizing thin melanomas: a case-control study of 43 cases by Guitart, Joan, Lowe, Lori, Piepkorn, Michael, Prieto, Victor G, Rabkin, Michael S, Ronan, Salve G, Shea, Christopher R, Tron, Victor A, White, Wain, Barnhill, Raymond L

    Published in Archives of dermatology (1960) (01-05-2002)
    “…To study clinical and histological features associated with metastasizing thin melanomas (MTMs). Case-control study of clinicopathological features of patients…”
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