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1.
JAMA Dermatol ; 159(6): 669-671, 2023 06 01.
Artículo en Inglés | MEDLINE | ID: mdl-37043228

RESUMEN

This case report describes a woman in her 50s with a large, crusted, erythematous plaque on the right chest that was consistent with a Hailey-Hailey disease flare.


Asunto(s)
Pénfigo Familiar Benigno , Humanos , Cinacalcet/uso terapéutico , Pénfigo Familiar Benigno/diagnóstico , Pénfigo Familiar Benigno/tratamiento farmacológico , Pomadas , Tacrolimus
2.
Pediatr Dermatol ; 39(6): 992-994, 2022 Nov.
Artículo en Inglés | MEDLINE | ID: mdl-35739629

RESUMEN

Microcystic lymphatic malformation (MiLM), also known as lymphangioma circumscriptum, is a superficial collection of lymphatic vessels measuring <1 cm in the largest diameter, often with a more extensive deeper malformation. It commonly presents as discrete or grouped plaques of clear or hemorrhagic vesicles classically described as "frogspawn"; however, here we describe a case of its unique presentation as firm papules on the lips of a healthy six-year-old child. These skin-colored papules in the absence of vesicles with lymphatic and/or hemorrhagic fluid may not be clinically indicative of MiLM. This case represents a diagnostic challenge due to the unique morphology of pink, fleshy papules as opposed to the clear or hemorrhagic vesicles typically observed in MiLM.


Asunto(s)
Quistes , Linfangioma , Anomalías Linfáticas , Niño , Humanos , Labio , Anomalías Linfáticas/diagnóstico , Linfangioma/diagnóstico , Vesícula , Hemorragia
3.
Case Rep Dermatol Med ; 2019: 1840280, 2019.
Artículo en Inglés | MEDLINE | ID: mdl-31687220

RESUMEN

Patients who suffer from rare skin diseases may try numerous therapies with many potential side effects before achieving remission. Livedoid vasculopathy (LV) is one such rare disease that lacks a definitive treatment as evidenced by randomized controlled trials. Although corticosteroids help reduce the pain flares associated with LV, they come at the risk of immunosuppression. We present a case of disseminated cutaneous infection of M. chelonae/abscessus arising in a diabetic patient on long-term corticosteroid therapy. This patient required an intensive antibiotic regimen and potentially lifelong antibiotic suppression pending improvement of her disseminated cutaneous infection. We report this case to increase awareness of the diagnostic consideration of atypical, rapidly growing mycobacterial (RGM) infection when encountering patients with a diffuse onset of ulcerative skin nodules amid a background of diabetes and long-term corticosteroid use.

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