Derm
Necrobiosis Lipoidica
search
Necrobiosis Lipoidica
, Necrobiosis Lipoidica diabeticorum
See Also
Skin Conditions in Diabetes Mellitus
Acanthosis Nigricans
Diabetic Dermopathy
Granuloma Annulare
Diabetic Ulcer
Diabetes Mellitus
Type I Diabetes Mellitus
Type II Diabetes Mellitus
Insulin Resistance Syndrome
Glucose Metabolism
Diabetes Mellitus Education
Diabetes Mellitus Complications
Diabetic Ketoacidosis
Hyperosmolar Hyperglycemic State
Diabetes Mellitus Control in Hospital
Diabetes Mellitus Glucose Management
Hypertension in Diabetes Mellitus
Hyperlipidemia in Diabetes Mellitus
Diabetic Retinopathy
Diabetic Nephropathy
Diabetic Neuropathy
Epidemiology
Age of onset
Type I Diabetes Mellitus
: 22 (mean age of onset)
Type II Diabetes Mellitus
: 30 to 50 years
Most common in women by 3 fold
Pathophysiology
Unknown etiology
Appears related to microvascular changes
Associated Conditions
Diabetes Mellitus
Necrobiosis patients with comorbid diabetes: 11-65%
Prevalence
of necrobiosis in Diabetes: 0.3 to 1.6%
Necrobiosis predicts of future diabetes development
Symptoms
Lesions are painless in most cases
Signs
Slowly growing oval atrophic
Plaque
s
May be several centimeters in size
Initial
Erythematous
Plaque
with raised irregular border
Later
Yellow brown waxy central atrophic area
Distribution
Classic (Diabetes): Bilateral shins, medial malleolus
Other less-commonly involved locations
Hands and
Forearm
s
Face and scalp
Abdomen
Telangiectases
(subcutaneous vessels)
Lesions may ulcerate with
Trauma
(risk of infection)
Associated
Neuropathy
in 50% of patients
Decreased pinprick and fine
Touch Sensation
Labs
Biopsy (often not needed)
Necrobiosis of
Collagen
Histiocytes and
Lymphocyte
s surround
Collagen
Inflammation around blood vessels
Differential Diagnosis
Dermatopathology
Granuloma Annulare
Clinical
Rheumatoid
Nodule
s in
Rheumatoid Arthritis
Erythema Nodosum
Management
Corticosteroid
s
Clobetasol Propionate
under
Occlusion
for 6 weeks
Intralesional
Kenalog
10 mg/ml (dilute to 2.5 mg/ml)
Oral
Prednisone
for 5 weeks
Topical Psoralen with
Ultraviolet A
Exposure (PUVA)
Inhibition of
Platelet
aggregation
Pentoxifylline
(
Trental
) 400 mg PO tid for 4-8 weeks
Aspirin
325 mg PO qd for 3 to 7 months
Dipyridamole
(
Persantine
) 150-200 mg PO divided qid
Skin Grafting or local excision
Not recommended due to high recurrence rate
Extensive skin involvement refractory to above
Other treatment modalities
Laser treatment for
Telangiectasia
s
Benzoyl Peroxide
for ulcerated lesions
Course
Gradually resolves over 6-12 year period
Residual atrophy persists after resolution
References
Habif (1996) Clinical Dermatology, Mosby, p. 784-5
Ferringer (2002) Dermatol Clin 20(3):483 [PubMed]
Lowitt (1991) J Am Acad Dermatol 25:735-48 [PubMed]
Paron (2000) Prim Care 27(2):371-83 [PubMed]
Type your search phrase here