Four cases of acute infectious urticaria showing significant elevation of plasma D‐dimer level

D‐dimer, a fibrinolytic end‐product, has been regarded as a biomarker indicating the severity of urticaria, especially in chronic urticaria. Regarding acute urticaria, D‐dimer level is also suggested to be elevated, which may be significant in comparison with chronic urticaria. However, the clinical features of acute urticaria with concomitant significant elevation of D‐dimer level have not been investigated in detail so far. We present four cases of acute urticaria fulfilling the proposed diagnostic criterion of acute infectious urticaria, in which significant elevation of D‐dimer level and rapid spontaneous normalization in parallel with the resolution of fever and urticaria occurs. No cases had deep vein thrombosis, disseminated intravascular coagulation and malignancy. All cases responded well to antihistaminic treatment in combination with antibiotics, and their fever and urticaria resolved within 10 days. All cases showed severe wheals persistent for several days resolving with hyperpigmentation. Histologically, infiltration into blood vessel walls and interstitial infiltration of lymphocytes and polymorphonuclear cells were marked in the dermis. In our cases, clinical features accorded with acute infectious urticaria, and their histological features were similar to those of neutrophilic urticaria as described previously. In conclusion, there is a certain group of acute urticaria associated with significant elevation of D‐dimer level. These common features of our cases may be characteristic in acute urticaria showing the coagulative and fibrinolytic abnormalities.

[1]  Y. Yanase,et al.  Histamine and Toll-like receptor ligands synergistically induce endothelial cell gap formation by the extrinsic coagulating pathway. , 2017, The Journal of allergy and clinical immunology.

[2]  Toshihiro Tanaka,et al.  Infectious urticaria complicated with intestinal edema , 2017, The Journal of dermatology.

[3]  B. Jilma,et al.  D-dimer and histamine in early stage bacteremia: A prospective controlled cohort study. , 2015, European journal of internal medicine.

[4]  W. V. van Heerde,et al.  Alterations of coagulation and fibrinolysis in patients with angioedema due to C1‐inhibitor deficiency , 2012, Clinical and experimental immunology.

[5]  M. Shima,et al.  Increase of coagulation potential in chronic spontaneous urticaria , 2011, Allergy.

[6]  Y. Kameyoshi,et al.  Coagulation/fibrinolysis and inflammation markers are associated with disease activity in patients with chronic urticaria , 2010, Allergy.

[7]  D. Fanoni,et al.  Expression of Tissue Factor by Eosinophils in Patients with Chronic Urticaria , 2008, International Archives of Allergy and Immunology.

[8]  K. Fujii,et al.  Elevation of circulating thrombin–antithrombin III complex and fibrin degradation products in urticaria: A laboratory finding unrelated to intravascular coagulopathy , 2008, The Journal of dermatology.

[9]  R. Asero,et al.  Severe chronic urticaria is associated with elevated plasma levels of D‐dimer , 2007, Allergy.

[10]  D. Fanoni,et al.  Activation of the tissue factor pathway of blood coagulation in patients with chronic urticaria. , 2007, The Journal of allergy and clinical immunology.

[11]  R. Asero,et al.  Plasma of patients with chronic urticaria shows signs of thrombin generation, and its intradermal injection causes wheal-and-flare reactions much more frequently than autologous serum. , 2006, The Journal of allergy and clinical immunology.

[12]  K. Nishioka,et al.  Infectious urticaria with purpura: a mild subtype of urticarial vasculitis? , 2005, Acta dermato-venereologica.

[13]  F. Furukawa,et al.  Acute Infectious Urticaria: Clinical and Laboratory Analysis in Nineteen Patients , 2000, The Journal of dermatology.

[14]  Haas,et al.  Neutrophilic urticaria: clinical features, histological changes and possible mechanisms , 1998, The British journal of dermatology.

[15]  M. Tharp Chronic urticaria: pathophysiology and treatment approaches. , 1996, The Journal of allergy and clinical immunology.