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1.
Sultan Qaboos Univ Med J ; 23(2): 256-258, 2023 May.
Artigo em Inglês | MEDLINE | ID: mdl-37377818

RESUMO

Primary systemic vasculitis can present with a wide spectrum of manifestations ranging from systemic non-specific features such as fever, malaise, arthralgia and myalgia to specific organ damage. We describe two cases of cholesterol embolisation syndrome and Kaposi sarcoma mimicking primary systemic vasculitis, both of which were characterised by features such as livedo reticularis, blue toe syndrome, a brown purpuric skin rash and positive perinuclear anti-neutrophil cytoplasmic antibodies associated with Kaposi sarcoma. Establishing the right diagnosis was challenging and thus this report aimed to highlight the possible ways to distinguish them from primary systemic vasculitis.


Assuntos
Síndrome do Artelho Azul , Livedo Reticular , Sarcoma de Kaposi , Vasculite Sistêmica , Humanos , Síndrome do Artelho Azul/complicações , Sarcoma de Kaposi/diagnóstico , Sarcoma de Kaposi/complicações , Livedo Reticular/etiologia , Livedo Reticular/patologia , Vasculite Sistêmica/complicações
2.
Neurosurg Rev ; 46(1): 146, 2023 Jun 24.
Artigo em Inglês | MEDLINE | ID: mdl-37354243

RESUMO

Cranial irradiation is associated with several adverse events such as endocrinopathy, growth retardation, neurocognitive impairment, secondary malignancies, cerebral vasculopathy, and potential stroke. The better side effects profile of proton beam therapy compared with that of photon radiation therapy is due to its physical properties, mainly the sharp dose fall-off after energy deposition in the Bragg peak. Despite the better toxicity profile of proton beam therapy, the risk of  moyamoya syndrome still exists. We conducted a systematic review of the existing literature on moyamoya syndrome after receiving cranial radiation therapy for pediatric brain tumors to investigate the incidence of moyamoya syndrome after receiving photon versus proton radiation therapy. In this review, we report that the incidence of moyamoya syndrome after receiving proton beam therapy is almost double that of photon-induced moyamoya syndrome. Patients who received proton beam therapy for the management of pediatric brain tumors are more likely to develop moyamoya syndrome at the age of less than 5 years. Meanwhile, most patients with proton-induced moyamoya are more likely to be diagnosed within the first 2 years after the completion of their proton beam therapy.


Assuntos
Neoplasias Encefálicas , Doença de Moyamoya , Terapia com Prótons , Criança , Humanos , Pré-Escolar , Terapia com Prótons/efeitos adversos , Doença de Moyamoya/epidemiologia , Doença de Moyamoya/etiologia , Prótons , Incidência , Neoplasias Encefálicas/complicações
3.
Cureus ; 13(11): e19529, 2021 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-34934549

RESUMO

Vaccine-related erythema nodosum is uncommon, especially after the coronavirus disease 2019 (COVID-19) vaccine. This study presents the first case of the Pfizer vaccine associated with erythema nodosum. A 22-year-old healthy woman presented with a five-day history of several red painful areas with swelling in the lower extremities that started one day after receiving the first dose of Pfizer vaccine. Past medical history, laboratory investigation, and chest radiograph revealed normal results. Erythema nodosum is an immune reaction that manifests as multiple, painful nodules commonly seen on the shin that resolved spontaneously two to eight weeks after the onset. In the absence of laboratory and chest radiograph abnormalities and shortly after receiving the Pfizer vaccine, vaccine-related erythema nodosum is the only possible explanation.

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