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2.
J Cutan Pathol ; 48(6): 739-744, 2021 Jun.
Article in English | MEDLINE | ID: mdl-33617003

ABSTRACT

BACKGROUND: The distinction between chondrodermatitis nodularis helicis (CNH) and hyperplastic actinic keratosis (HAK) on the ear can pose a diagnostic challenge. We aimed to identify histopathological characteristics that could distinguish between CNH and HAK on routine sections using penalized least absolute shrinkage and selection operator (LASSO) logistic regression analysis. METHODS: Cases of CNH (n = 80) and HAK (n = 28) were analyzed for selected histopathological characteristics. Fisher's exact test and LASSO regression were performed. RESULTS: In univariate analyses, the following were significantly associated with CNH: ulceration, acanthosis, granular layer in the majority of the lesion, hypergranulosis at the periphery of the lesion, hyperkeratosis at the periphery of the lesion, hyperparakeratosis at the periphery of the lesion, fibrosis, increased blood vessels, vertically oriented blood vessels, and fibrin. A LASSO model excluding atypia found that fibrin, fibrosis, presence of granular layer, ulceration, and vertically oriented blood vessels were most predictive of CNH. Keratinized strap cells were not a significant predictor. CONCLUSION: We have identified features that may aid in differentiating these entities and demonstrated that a LASSO regression model can identify predictors that may improve diagnostic accuracy. Our results indicate that the highest diagnostic accuracy in this dilemma is dependent on obtaining biopsy specimens with visible dermis.


Subject(s)
Cartilage Diseases/pathology , Dermatitis/pathology , Hyperplasia/pathology , Keratosis, Actinic/pathology , Biopsy , Diagnosis, Differential , Ear/pathology , Fibrosis/pathology , Humans , Keratosis, Actinic/diagnosis , Logistic Models , Neovascularization, Pathologic/pathology , Prurigo/diagnosis , Prurigo/pathology , Retrospective Studies
5.
Dermatol Online J ; 25(10)2019 Oct 15.
Article in English | MEDLINE | ID: mdl-31735009

ABSTRACT

Hydroxyurea is a chemotherapeutic agent that is used in the treatment of various hematological diseases including chronic myelogenous leukemia, polycythemia vera, and sickle cell anemia. Hydroxyurea is also used to treat psoriasis. Drug-induced hyperpigmentation is a known cutaneous side effect of hydroxyurea along with xerosis, dermal ulcers, and dermatomyositis-like eruptions. Hyperpigmentation has been observed in the oral mucosa, nails, and in a generalized or a diffuse pattern. The mechanism of hyperpigmentation related to hydroxyurea is believed to be correlated with increased melanin. Classically, clinical types of diffuse hyperpigmentation owing to iron deposition in the dermis have been associated with minocycline and not with hydroxyurea. We report a novel case in which hydroxyurea hyperpigmentation is associated with iron deposition.


Subject(s)
Hydroxyurea/adverse effects , Hyperpigmentation/chemically induced , Iron/analysis , Nucleic Acid Synthesis Inhibitors/adverse effects , Skin/pathology , Aged , Humans , Hyperpigmentation/pathology , Male , Microscopy, Electrochemical, Scanning , Skin/chemistry
7.
J Cutan Med Surg ; 22(4): 424-426, 2018.
Article in English | MEDLINE | ID: mdl-29502440

ABSTRACT

Sarcoidosis is a multisystem inflammatory condition of unknown etiology. Variability in the cutaneous features of sarcoidosis is profound, and its protean manifestations affirm the condition's designation as one of dermatology's "great mimics." Cutaneous phenotypes of sarcoidosis include but are by no means limited to ichthyosiform, alopecic, erythrodermic, angiolupoid, and verrucous variants. Verrucous sarcoidosis is an exceedingly rare manifestation, and previous reports of this phenotype are limited to 15 cases. Most cases in the extant literature presented on the extremities, with clinical features mimicking that of a common wart, or as verrucous crateriform nodules, ulcers, or cutaneous horns. Only 4 previous reports of facial verrucous sarcoidosis exist in the literature, and to our knowledge, no prior cases have demonstrated filiform lesion morphology. Here we present a case of filiform verrucous sarcoidosis in an otherwise healthy, middle-aged African American man, devoid of internal organ involvement and limited to the face, histopathologically confirmed by the presence of characteristic granulomata devoid of lymphocytic infiltrates.


Subject(s)
Face/pathology , Sarcoidosis , Skin/pathology , Warts , Humans , Male , Middle Aged
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