Eruptive pseudoangiomatosis in adults with immune system disorders: A report of two cases
Eruptive pseudoangiomatosis is a cutaneous disease of unknown origin, characterized by the sudden appearance of small, asymptomatic angioma-like erythematous papules surrounded by a pale halo that resolves spontaneously. It occurs due to transitory dermal blood vessel dilation and has been associat...
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doaj-bff61cbbdf214db6ac66661595c999852021-02-02T11:34:58ZengPAGEPress PublicationsDermatology Reports2036-73922036-74062020-12-0112310.4081/dr.2020.8836Eruptive pseudoangiomatosis in adults with immune system disorders: A report of two casesSandra González Saldaña0Raul G. Mendez Flores1Andrea F. López Gutiérrez2Lupita N. Salas Núñez3Ana Karen Hermosillo Loya4Marisol Ramírez Padilla5Mercedes Hernández Torres6Department of Dermatology, Civil Hospital of Guadalajara, JaliscoDepartment of Dermatology, Civil Hospital of Guadalajara, JaliscoDepartment of Dermatology, Civil Hospital of Guadalajara, JaliscoDepartment of Dermatology, Civil Hospital of Guadalajara, JaliscoDepartment of Dermatology, Civil Hospital of Guadalajara, JaliscoDepartment of Dermatology, Civil Hospital of Guadalajara, JaliscoPrivate Practice Dermatopathology, Guadalajara Eruptive pseudoangiomatosis is a cutaneous disease of unknown origin, characterized by the sudden appearance of small, asymptomatic angioma-like erythematous papules surrounded by a pale halo that resolves spontaneously. It occurs due to transitory dermal blood vessel dilation and has been associated with viral infections and hematologic disorders. To this day, it remains a disease that affects mostly the lower spectrum of life. Most of the cases have been reported in children and few reports have described its association with immune system disorders. The diagnosis is based upon clinical presentation. Histopathological analysis has no pathognomonic findings and can include dilated dermal blood vessels, perivascular lymphocytic infiltration and plump endothelial cells. We report a 21-years-old female diagnosed with HIV in AIDS stage and a 19- years-old male diagnosed with non- Hodgkin’s lymphoma. https://www.pagepress.org/journals/index.php/dr/article/view/8836Eruptive pseudoangiomatosisimmune system disordersHIVnon-hodgkin lymphoma |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Sandra González Saldaña Raul G. Mendez Flores Andrea F. López Gutiérrez Lupita N. Salas Núñez Ana Karen Hermosillo Loya Marisol Ramírez Padilla Mercedes Hernández Torres |
spellingShingle |
Sandra González Saldaña Raul G. Mendez Flores Andrea F. López Gutiérrez Lupita N. Salas Núñez Ana Karen Hermosillo Loya Marisol Ramírez Padilla Mercedes Hernández Torres Eruptive pseudoangiomatosis in adults with immune system disorders: A report of two cases Dermatology Reports Eruptive pseudoangiomatosis immune system disorders HIV non-hodgkin lymphoma |
author_facet |
Sandra González Saldaña Raul G. Mendez Flores Andrea F. López Gutiérrez Lupita N. Salas Núñez Ana Karen Hermosillo Loya Marisol Ramírez Padilla Mercedes Hernández Torres |
author_sort |
Sandra González Saldaña |
title |
Eruptive pseudoangiomatosis in adults with immune system disorders: A report of two cases |
title_short |
Eruptive pseudoangiomatosis in adults with immune system disorders: A report of two cases |
title_full |
Eruptive pseudoangiomatosis in adults with immune system disorders: A report of two cases |
title_fullStr |
Eruptive pseudoangiomatosis in adults with immune system disorders: A report of two cases |
title_full_unstemmed |
Eruptive pseudoangiomatosis in adults with immune system disorders: A report of two cases |
title_sort |
eruptive pseudoangiomatosis in adults with immune system disorders: a report of two cases |
publisher |
PAGEPress Publications |
series |
Dermatology Reports |
issn |
2036-7392 2036-7406 |
publishDate |
2020-12-01 |
description |
Eruptive pseudoangiomatosis is a cutaneous disease of unknown origin, characterized by the sudden appearance of small, asymptomatic angioma-like erythematous papules surrounded by a pale halo that resolves spontaneously. It occurs due to transitory dermal blood vessel dilation and has been associated with viral infections and hematologic disorders. To this day, it remains a disease that affects mostly the lower spectrum of life. Most of the cases have been reported in children and few reports have described its association with immune system disorders. The diagnosis is based upon clinical presentation. Histopathological analysis has no pathognomonic findings and can include dilated dermal blood vessels, perivascular lymphocytic infiltration and plump endothelial cells. We report a 21-years-old female diagnosed with HIV in AIDS stage and a 19- years-old male diagnosed with non- Hodgkin’s lymphoma.
|
topic |
Eruptive pseudoangiomatosis immune system disorders HIV non-hodgkin lymphoma |
url |
https://www.pagepress.org/journals/index.php/dr/article/view/8836 |
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