2010
DOI: 10.1111/j.1365-2133.2010.09829.x
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Chilblains and antiphospholipid antibodies: report of four cases and review of the literature

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Cited by 17 publications
(10 citation statements)
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“…9,[12][13][14] Chilblains may Goutières syndrome, and IRAK4 deficiency); and (f) anorexia and diseases causing weight reduction. 10,15,16 None of these possible etiologies were present in our patients, not even cold exposure, and given the timing, SARS-CoV-2 is felt to be the most likely etiology of chilblains in these patients. Five of our patients were receiving medications for ADHD, and these have been linked to blue toe syndrome and cyanotic peripheral vasculopathy.…”
Section: Re Sultsmentioning
confidence: 65%
“…9,[12][13][14] Chilblains may Goutières syndrome, and IRAK4 deficiency); and (f) anorexia and diseases causing weight reduction. 10,15,16 None of these possible etiologies were present in our patients, not even cold exposure, and given the timing, SARS-CoV-2 is felt to be the most likely etiology of chilblains in these patients. Five of our patients were receiving medications for ADHD, and these have been linked to blue toe syndrome and cyanotic peripheral vasculopathy.…”
Section: Re Sultsmentioning
confidence: 65%
“…Indeed, this process may not represent a forme fruste but rather may actually represent cutaneous LE involving acral skin without any associated systemic disease, akin to tumid and discoid LE, in which most of these cases have no association with systemic disease. In addition, chilblain and a chilblain‐like eruption have been reported in patients with antiphopholipid antibodies, Behcet's disease, and hematologic malignancy, mainly leukemia . In 13 reported patients with chilblain and antiphospholipid antibodies, 2 developed systemic LE and 9 had primary antiphopholipid syndrome …”
Section: Discussionmentioning
confidence: 99%
“…In addition, chilblain and a chilblain‐like eruption have been reported in patients with antiphopholipid antibodies, Behcet's disease, and hematologic malignancy, mainly leukemia . In 13 reported patients with chilblain and antiphospholipid antibodies, 2 developed systemic LE and 9 had primary antiphopholipid syndrome …”
Section: Discussionmentioning
confidence: 99%
“…2,3 Chilblains can can present as a secondary feature of diseases such as systemic lupus erythematosus, Behçet disease, chronic myelomonocytic leukemia, metastatic breast carcinoma, cryoglobulinemia, cryofibrinogenemia, cold agglutinin disease, macroglobulinemia, Aicardi-Goutieres syndrome and anorexia nervosa. 4,5 Laboratory investigations and cutaneous biopsy may be performed when lesions are persistent or when there is suspicion of underlying systemic disease.…”
Section: Introductionmentioning
confidence: 99%