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215


Paraneoplastic microscopic polyangiitis presenting after thymectomy [Case Report]

Tracey, Elisabeth H; Huen, Auris O; Sreih, Antoine G; Evans, Tracey; Kobrin, Sidney; Rubin, Adam I; Rosenbach, Misha
PMCID:4864238
PMID: 27222874
ISSN: 2352-5126
CID: 5748022

Ice-pack Dermatosis: A Diagnositic Pitfall for Dermatopathologists that Mimics Lupus Erythematosus

Haber, Jessica S; Ker, Khor Jia; Werth, Victoria P; Rubin, Adam
PMID: 26818895
ISSN: 1600-0560
CID: 2043992

Iatrogenic Necrolytic Migratory Erythema in an Infant with Congenital Hyperinsulinism [Case Report]

Coughlin, Carrie C; Roy, Sani M; Arkin, Lisa M; Adzick, N Scott; Yan, Albert C; De León, Diva D; Rubin, Adam I
Necrolytic migratory erythema (NME) is a rare cutaneous finding characterized by painful, pruritic, scaly red patches and plaques, bullae, and superficial erosions. Typically NME is a paraneoplastic phenomenon associated with glucagonoma. We report the exceptional case of an infant who developed iatrogenic NME arising secondary to glucagon therapy for congenital hyperinsulinism.
PMID: 26648573
ISSN: 1525-1470
CID: 5748002

Wells’ Syndrome

Chapter by: Jen, M; Rubin, Adam I
in: Hematopathology of the Skin: Clinical and Pathological Approach by Gru; Alejandro Ariel, Schaffer, Andras[Ed.]
Wolters Kluwer Health
pp. -
ISBN: 9781496300584
CID: 5751142

Dramatic improvement of yellow nail syndrome with a combination of intralesional triamcinolone, fluconazole, and sinusitis management [Letter]

Imadojemu, Sotonye; Rubin, Adam
PMID: 26226835
ISSN: 1365-4632
CID: 5747972

Disseminated coccidioidomycosis masquerading as a ruptured epidermal inclusion cyst in a healthy young adult from Philadelphia [Letter]

Farber, Sara A; Rubin, Adam I; Micheletti, Robert G
PMID: 26267257
ISSN: 1365-4632
CID: 5747982

Polydactylous Longitudinal Melanonychia Acquired following Total Skin Electron Beam Radiation Therapy for Sézary Syndrome

Cedeno-Laurent, Filiberto; Kim, Ellen J; Rook, Alain H; Vittorio, Carmela C; Rubin, Adam I
PMCID:4857819
PMID: 27170936
ISSN: 2296-9195
CID: 5748012

Routine nail clipping leads to the diagnosis of amelanotic nail unit melanoma in a young construction worker [Case Report]

Boni, Andrea; Chu, Emily Y; Rubin, Adam I
PMID: 26272255
ISSN: 1600-0560
CID: 5747992

Inflammatory diseases of the nail unit

Hinshaw, Molly A; Rubin, Adam
inflammatory disorders of the nail unit are frequently encountered in clinical medicine and are a cause of significant morbidity. Psoriasis, lichen planus, chronic paronychia, and trachyonychia will be discussed. An approach to diagnosis and management of these disorders requires knowledge of nail unit anatomy, consideration of associated systemic manifestations, and patient education with respect to prognosis and management of factors that will maximize disease improvement. The nail unit responds with a limited number of signs to disparate clinical entities such that there is some overlap in clinical presentation between inflammatory conditions. Nail unit biopsy may therefore be useful in establishing a specific diagnosis.
PMID: 26176289
ISSN: 1085-5629
CID: 5747962

Myxoid onychomatricoma: an unusual variant of a rare nail unit tumor [Case Report]

Stewart, Campbell L; Sobanko, Joseph F; Rubin, Adam I
A 57-year-old woman presented with a 3-year history of a thickened, yellowed, over-curved nail plate of the left second toe. The proximal nail fold had an associated nodule. When observed head-on, the distal nail plate demonstrated multiple circular perforations. Avulsion of the nail plate revealed a 0.7 cm pale white mass within the proximal nail matrix, which was excised. Histologic sections of the nail plate showed longitudinal cystic spaces associated with papillary projections of nail matrix epithelium. The parenchyma of the lesion demonstrated bland-appearing spindled cells in a prominent myxoid stroma with abundant mast cells. The spindled cells were focally positive for CD34 and factor XIIIa and negative for S100, pan-cytokeratin, desmin, smooth muscle actin, epithelial membrane antigen, and MART-1. Onychomatricoma (OM) is a rare nail unit biphasic fibroepithelial tumor with multiple radiating digitations lined by papillomatous matrix epithelium. The epithelial component is consisted of matrix cells that generate the thickened nail plate, and the digitations cause characteristic "wormwood" perforations of the nail plate. A fibrous stroma is characteristic with staining positive for CD34 and negative for CD99, epithelial membrane antigen, and S100. This case is unique with the presence of a prominent myxoid stroma associated with the fibrous component of the OM. Only 1 previous report of OM highlights a related finding of a myxocollagenous stroma. This purely myxoid variant represents a new distinct form of OM. Clinicopathologic correlation is essential to avoid confusion with other myxoid tumors such as a superficial acral myxoma, superficial angiomyxoma, or a digital myxoid cyst.
PMID: 25830718
ISSN: 1533-0311
CID: 5747932