Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 5 de 5
Filter
Add more filters










Database
Language
Publication year range
1.
Am J Dermatopathol ; 45(7): 478-481, 2023 Jul 01.
Article in English | MEDLINE | ID: mdl-37249361

ABSTRACT

ABSTRACT: Sarcoidosis is an idiopathic multisystem inflammatory disease that can affect virtually any part of the body. Often, it can initially present solely in the skin. Histologically, it is characterized by noncaseating, 'naked' granulomas in the dermis and subcutaneous tissue. Clinically, sarcoidosis is often referred to as a 'mimicker' of many other pathologic processes because of its wide array of presentations. Occasionally, sarcoidosis can present in the scalp as both a scarring and nonscarring alopecia. There are countless reports of sarcoidosis mimicking various other alopecias including acne keloidalis nuchae, discoid lupus erythematosus, frontal fibrosing alopecia, lichen planopilaris, and alopecia areata totalis. In this case series, we present 2 novel cases of sarcoidosis not just clinically mimicking other forms of alopecia but occurring in conjunction with a separate and histologically distinct primary alopecia.


Subject(s)
Alopecia Areata , Lichen Planus , Sarcoidosis , Humans , Alopecia/pathology , Alopecia Areata/complications , Alopecia Areata/pathology , Cicatrix/pathology , Lichen Planus/pathology , Sarcoidosis/complications , Sarcoidosis/pathology , Scalp/pathology
3.
J Cutan Pathol ; 47(10): 967-969, 2020 Oct.
Article in English | MEDLINE | ID: mdl-32447757

ABSTRACT

Structures resembling Meissner corpuscles have been described in various nerve sheath tumors, including schwannomas and neurofibromas. When present, they are focal or scattered, and rarely a prominent feature of the lesion. Here, we report a case of a 39-year-old female who presented with an isolated lesion on her abdomen. Histopathologically, the tumor was almost exclusively composed of Meissner corpuscle-like structures (pseudo-meissnerian bodies). At a small edge of the tumor, there were features of a classic neurofibroma, with a mixture of Schwann cells, fibroblast-like cells, and interspersed mast cells. We propose the term "meissnerian neurofibroma" for this extremely rare variant of neurofibroma.


Subject(s)
Mechanoreceptors/pathology , Nerve Sheath Neoplasms/pathology , Neurofibroma/pathology , Adult , Diagnosis, Differential , Female , Fibroblasts/pathology , Humans , Mast Cells/pathology , Neurilemmoma/diagnosis , Neurilemmoma/pathology , Neurofibroma/diagnosis , Neurofibroma/metabolism , S100 Proteins/metabolism , Schwann Cells/pathology
SELECTION OF CITATIONS
SEARCH DETAIL
...