Publications by authors named "Erin Huiras"

Purpose Of Review: The introduction of highly active antiretroviral therapy (HAART) has altered the pattern of dermatologic disease among HIV-infected patients. While the majority benefit substantially from highly active antiretroviral therapy-induced immune recovery, a subset of patients experience unmasking of new skin disease or paradoxical worsening of existing dermatologic conditions, attributable to immune reconstitution inflammatory syndrome. We review the current literature regarding the dermatologic manifestations of immune reconstitution inflammatory syndrome.

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Article Synopsis
  • Plaque-type syringoma is a rare benign tumor often misidentified as microcystic adnexal carcinoma (MAC), which can lead to unnecessary and potentially harmful surgeries.
  • The study presents two cases of plaque-type syringoma initially diagnosed as MAC, highlighting microscopic features that distinguish it from MAC, such as the arrangement of cuboidal cells and the lack of deeper tissue involvement.
  • The report emphasizes the importance of accurate histopathologic diagnosis, discussing key findings and cases of plaque-type syringoma documented in medical literature.
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Bacillary angiomatosis is an opportunistic bacterial infection caused by either Bartonella henselae or B. quintana. The classic histologic presentation of bacillary angiomatosis involves three components: a lobular proliferation of capillaries with enlarged endothelial cells, neutrophilic debris, and clumps of finely granular material identified as bacteria with staining techniques.

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Klippel-Trenaunay syndrome (KTS) is a rare congenital anomaly characterized by unilateral limb overgrowth, venous varicosities, and capillary malformations (port wine stains) of the affected limb or limbs. Large venous malformations such as those observed in KTS are rare, and many physicians are unfamiliar with the potential complications, which include hypercoagulability, thrombosis, and pulmonary embolism (PE). As a result, patients may suffer from delayed diagnosis of a potentially life-threatening thromboembolic event.

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