Azathioprine hypersensitivity syndrome. Report of two cases with cutaneous manifestations

Author(s):  
C. Moya‐Martínez ◽  
L. Núñez‐Hipólito ◽  
S. Barrio‐González ◽  
C. Santonja ◽  
M.J. Velasco ◽  
...  
2021 ◽  
Vol 14 (5) ◽  
pp. e239099
Author(s):  
Tahlia McKenzie ◽  
Shyam Dheda ◽  
Murty Mantha ◽  
Catherine Larsen

Azathioprine hypersensitivity syndrome is a rare but potentially severe side effect of azathioprine use. It has a variable and non-specific presentation making it difficult to distinguish from sepsis or disease relapse. High clinical suspicion is therefore required for recognition and prompt cessation of azathioprine for symptom resolution. Herewith two cases of severe azathioprine hypersensitivity syndrome are described, one in association with Sweet syndrome. Both presented with vague symptoms 2 weeks after commencing azathioprine for antineutrophil cytoplasmic antibody vasculitis. The differentials of sepsis and disease relapse were considered prior to cessation of azathioprine which resulted in a dramatic improvement in both cases. These cases highlight the diagnostic challenge azathioprine hypersensitivity syndrome presents. It should be suspected when there is a temporal relationship to drug initiation, with absence of infection or serological evidence of disease relapse.


2013 ◽  
Vol 30 (6) ◽  
pp. 665-673 ◽  
Author(s):  
Fanny Morice-Picard ◽  
Khaled Ezzedine ◽  
Marie-Ange Delrue ◽  
Benoit Arveiler ◽  
Patricia Fergelot ◽  
...  

2012 ◽  
Vol 153 (15) ◽  
pp. 586-591 ◽  
Author(s):  
Ágnes Kinyó ◽  
Anna Lakatos ◽  
Anita Varga ◽  
Roland Gyulai ◽  
Erika Varga ◽  
...  

Allopurinol is an effective urate lowering drug, which is usually well-tolerated with no adverse effects in most cases, but about 2% of the treated patients develop a skin rash, and patients may experience severe allopurinol-induced hypersensitivity syndrome. Aims: The aim of the authors was to summarize and present the clinical manifestations of allopurinol-induced hypersensitivity in patients treated at the Department of Dermatology and Allergology, University of Szeged in order to identify potential associations with this syndrome. Methods: Retrospective review of all patients who were referred to the department with allopurinol-induced hypersensitivity syndrome in the last four years. Results: During four years, 11 patients were treated with allopurinol-induced hypersensitivity syndrome. The average age was 70.3 years. Before the initiation of allopurinol therapy, 36% of patients had already suffered from various degrees of renal impairment, and 72% of them had been taking thiazide diuretics. Cutaneous manifestations were mainly generalized, erythematous, maculopapular exanthemas (9 patients, 82%), and two patients showed signs of erythema multiforme (18%). Asymptomatic hyperuricemia was the indication for allopurinol therapy in all patients. Conclusions: Allopurinol-induced hypersensitivity syndrome is a severe, life-threatening disease. Administration of allopurinol should be initiated with clear indications in appropriate dose. Old age, underlying renal impairment and concomitant thiazide diuretic intake should be considered as potential risk factors for developing hypersensitivity syndrome. Orv. Hetil., 2012, 153, 586–591.


2017 ◽  
Vol 2017 ◽  
pp. 1-5 ◽  
Author(s):  
Mari Orime

Diagnosis of severe cutaneous adverse drug reactions should involve immunohistopathological examination, which gives insight into the pathomechanisms of these disorders. The characteristic histological findings of erythema multiforme (EM), Stevens–Johnson syndrome (SJS), and toxic epidermal necrolysis (TEN) provide conclusive evidence demonstrating that SJS/TEN can be distinguished from EM. Established SJS/TEN shows full-thickness, extensive keratinocyte necrosis that develops into subepidermal bullae. Drug-induced hypersensitivity syndrome (DIHS) and exanthema in drug reaction with eosinophilia and systemic symptoms (DRESS) each display a variety of histopathological findings, which may partly correlate with the clinical manifestations. Although the histopathology of DRESS is nonspecific, the association of two or more of the four patterns—eczematous changes, interface dermatitis, acute generalized exanthematous pustulosis- (AGEP-) like patterns, and EM-like patterns—might appear in a single biopsy specimen, suggesting the diagnosis and severe cutaneous manifestations of DRESS. Cutaneous dendritic cells may be involved in the clinical course. AGEP typically shows spongiform superficial epidermal pustules accompanied with edema of the papillary dermis and abundant mixed perivascular infiltrates. Mutations in IL36RN may have a definite effect on pathological similarities between AGEP and generalized pustular psoriasis.


2003 ◽  
Vol 12 (3) ◽  
pp. 197-199 ◽  
Author(s):  
Hanan A. Bin-Nakhi ◽  
Sameera Sadeq ◽  
Raimond G. Pinto ◽  
Yousef Habeeb

2010 ◽  
Vol 30 (4) ◽  
pp. 573-580 ◽  
Author(s):  
Laura Bosco ◽  
Anna Peroni ◽  
Donatella Schena ◽  
Chiara Colato ◽  
Giampiero Girolomoni

Medicine ◽  
1995 ◽  
Vol 74 (3) ◽  
pp. 144-151 ◽  
Author(s):  
An S. P. De Vriese ◽  
Jan Philippe ◽  
Dirk M. Van Renterghem ◽  
Christa A. De Cuyper ◽  
Philippe H. F. Hindryckx ◽  
...  

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