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Acral manifestations of soft tissue tumors.
Abstract
This group of biologically diverse entities is united by topographic localization
to the hands and feet. Categorizing tumors by body site narrows the differential into
a short list of possibilities that can facilitate accurate and rapid diagnosis. The
goal of this review is to provide a practical approach to soft tissue tumors of acral
locations for clinicians, pathologists, and researchers alike. What ensues in the
following text is that tight coupling of the clinical picture and histopathologic
findings should produce the correct diagnosis, or at least an abbreviated differential.
The salient clinicopathologic, immunohistochemical, and molecular features are presented
alongside current treatment recommendations for each entity.
Type
Journal articlePermalink
https://hdl.handle.net/10161/13269Published Version (Please cite this version)
10.1016/j.clindermatol.2016.09.012Publication Info
Paral, KM; & Petronic-Rosic, V (2017). Acral manifestations of soft tissue tumors. Clin Dermatol, 35(1). pp. 85-98. 10.1016/j.clindermatol.2016.09.012. Retrieved from https://hdl.handle.net/10161/13269.This is constructed from limited available data and may be imprecise. To cite this
article, please review & use the official citation provided by the journal.
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Show full item recordScholars@Duke
Kristen Michelle Paral
Assistant Professor of Pathology
Dr. Kristen Paral is board-certified in Dermatopathology and Anatomic & Clinical Pathology.
She specializes in inflammatory and neoplastic disorders of the skin, soft tissues,
and bone.
This author no longer has a Scholars@Duke profile, so the information shown here reflects
their Duke status at the time this item was deposited.

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