scispace - formally typeset
G

George P. Lupton

Researcher at Walter Reed Army Institute of Research

Publications -  38
Citations -  1973

George P. Lupton is an academic researcher from Walter Reed Army Institute of Research. The author has contributed to research in topics: Nevus & Carcinoma. The author has an hindex of 23, co-authored 38 publications receiving 1899 citations.

Papers
More filters
Journal ArticleDOI

Merkel cell carcinoma: Analysis of clinical, histologic, and immunohistologic features of 132 cases with relation to survival

TL;DR: Cell size, mitotic rate, and tumor size are significant factors in relation to the biologic behavior of MCC.
Journal ArticleDOI

Spindle Cell and Epithelioid Cell Nevi with Atypia and Metastasis (Malignant Spitz Nevus)

TL;DR: Study of these cases suggests that although some lesions with features of S&E nevi may involve local lymph nodes, widespread metastases do not result, and no recurrences or further metastases have been found.
Journal ArticleDOI

Neurothekeoma: An Analysis of 178 Tumors With Detailed Immunohistochemical Data and Long-term Patient Follow-up Information

TL;DR: The clinicopathologic findings in 176 patients who presented with 178 tumors currently referred to as neurothekeomas are morphologically and immunohistochemically distinct from true nerve sheath myxomas.
Journal ArticleDOI

Aggressive digital papillary adenocarcinoma (aggressive digital papillary adenoma and adenocarcinoma revisited).

TL;DR: None of the clinical or histologic parameters studied were found to be predictive of recurrence or metastasis, indicating that the originally proposed criteria for distinguishing between benign (adenoma) and malignant (adenocarcinoma) do not predict biologic behavior.
Journal ArticleDOI

Hmb-45 Staining in Benign and Malignant Melanocytic Lesions: A Reflection of Cellular Activation

TL;DR: HMB-45 may correlate best with factors that stimulate melanocytic proliferation and production of melanosomes, and thus may correlate with melanosome production and thus a melanocytics origin of HMB- 45-positive cells.