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1.
Pediatr Dermatol ; 2024 Jul 05.
Artículo en Inglés | MEDLINE | ID: mdl-38967954

RESUMEN

Cutaneous pyogenic granulomas (PGs) are common, benign vascular tumors of uncertain pathogenesis; however, a growing body of literature suggests that the formation of PGs may be secondary to genetic alterations in both the Ras/Raf/MAPK and PI3K/Akt/mTOR pathways. We present three cases of spontaneous multifocal PGs that first presented in infancy, were not associated with other vascular anomalies or discernable etiology, harbored somatic genetic variants in the Ras/Raf/MAPK pathway (NRAS n = 2, FGFR1 n = 1), were refractory to treatment with beta-blockers and mTOR inhibitors, and responded best to pulsed dye laser. We propose the term "spontaneous multifocal PGs" to describe this entity.

2.
Dermatol Online J ; 28(3)2022 Jun 15.
Artículo en Inglés | MEDLINE | ID: mdl-36259802

RESUMEN

Lichen amyloidosis is believed to be caused by damage to keratinocytes, often by chronic scratching. It has also been associated with autoimmune conditions, including thyroid disease. Dermatologic manifestations of poorly controlled thyroid disease are well described within the medical literature, within both hypothyroid and hyperthyroid states. Myxedema is a rare complication of Graves disease. We report a unique case of concurrent myxedema and lichen amyloidosis in a 63-year-old patient with uncontrolled hypothyroidism in the setting of post-ablative Graves disease.


Asunto(s)
Amiloidosis Familiar , Enfermedad de Graves , Hipotiroidismo , Mixedema , Humanos , Persona de Mediana Edad , Mixedema/complicaciones , Mixedema/diagnóstico , Enfermedad de Graves/complicaciones , Amiloidosis Familiar/complicaciones , Amiloidosis Familiar/diagnóstico , Hipotiroidismo/complicaciones
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