Necrobiosis Lipoidica: Early Diagnosis and Treatment with Tacrolimus

We present a case of necrobiosis lipoidica (NL) with atypical early lesions and good response to topical tacrolimus. NL is a disease with clinical features that are seldom misinterpreted. Often histology just confirms the clinician's diagnosis. Only in rare cases, the clinical presentation and...

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Main Authors: A. Patsatsi (Author), A. Kyriakou (Author), D. Sotiriadis (Author)
Format: Book
Published: Karger Publishers, 2011-04-01T00:00:00Z.
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100 1 0 |a A. Patsatsi  |e author 
700 1 0 |a A. Kyriakou  |e author 
700 1 0 |a D. Sotiriadis  |e author 
245 0 0 |a Necrobiosis Lipoidica: Early Diagnosis and Treatment with Tacrolimus 
260 |b Karger Publishers,   |c 2011-04-01T00:00:00Z. 
500 |a 1662-6567 
500 |a 10.1159/000327936 
520 |a We present a case of necrobiosis lipoidica (NL) with atypical early lesions and good response to topical tacrolimus. NL is a disease with clinical features that are seldom misinterpreted. Often histology just confirms the clinician's diagnosis. Only in rare cases, the clinical presentation and the involved body sites may be misleading. A 67-year-old diabetic woman was admitted to our department with a well-defined, persistent plaque on her left arm and on her right shin. Histologic examination of both lesions revealed features of NL despite the dissimilar clinical presentation. The patient was treated with 0.1% topical tacrolimus ointment twice daily for 8 weeks and once daily for 8 weeks. A significant improvement and no further lesions were observed after 1 year of follow-up. A high index of suspicion regarding NL lesions with atypical clinical presentation on different body sites is advised in order to avoid misdiagnosis, wrong treatment decisions and ulceration. Additionally, it appears that topical tacrolimus treatment is an effective therapeutic option in patients with recent, non-ulcerated NL lesions. 
546 |a EN 
690 |a Diabetes 
690 |a Necrobiosis lipoidica 
690 |a Ulceration 
690 |a Dermatology 
690 |a RL1-803 
655 7 |a article  |2 local 
786 0 |n Case Reports in Dermatology, Vol 3, Iss 1, Pp 89-93 (2011) 
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