Talk:Necrobiotic granulomatous processes
Granuloma annulare[edit source]
It is a frequent benign chronic skin disease characterized histologically by the formation of necrobiotic granulomas, typical clinical manifestations are ring-shaped (annular) papules. The disease mainly affects children and young adults, more often women.
Etiology[edit source]
Unknown, in 20% it is associated with diabetes mellitus.
Clinical picture[edit source]
- Localized form - a hard reddish nodule, increases in the periphery with a palpable mass of closely grouped sharply demarcated papules; the center sinks in - the skin here has a normal appearance - the manifestation acquires an annular arrangement with a diameter of several centimeters without subjective symptoms; most often above the joints - mainly the backs of the hands, feet, on the fingers, around the ankles and elbows.
- Rare forms - disseminated, erythematous, subcutaneous, perforating.
Diagnosis[edit source]
Clinical appearance + histological evidence of necrobiotic granuloma; in the case of the disseminated form, diabetes mellitus must be ruled out.
Differential diagnosis[edit source]
Localized form – tinea, lichen planus annular form, sarcoidosis, lupus erythematodes.
Therapy[edit source]
Localized form – locally corticoids; systemic treatment is usually not necessary.
Progress[edit source]
Mostly spontaneous healing ad integrum within 1-2 years.
Necrobiosis lipoidica (diabeticorum)[edit source]
A chronic disease with the formation of necrobiotic granulomas, most often affecting the lower legs; about 1% of diabetics - up to 50% of patients with this disease have DM; most often middle-aged women.
Etiology[edit source]
Unknown, signs of small vessel damage may be related to diabetic microangiopathy; sometimes changes in the character of vasculitis.
Clinical picture[edit source]
Front sides of lower legs; sharply demarcated, mostly bilateral, indurated, smooth, shiny deposits to surfaces of various shapes, reddish-brown at the edges; the center is rather orange or yellowish with visible vascular ectasias; about 30% develop poorly healing ulcers.
Diagnosis[edit source]
Clinical appearance and typical localization, biopsy may lead to the formation of an ulcer.
Differential diagnosis[edit source]
Mainly granuloma annulare, other ulcers.
Therapy[edit source]
Mostly unsuccessful, local corticoids are tried in occlusion or intralesionally; microcirculation treatment – venotonics and rheology – sometimes leads to improvement.
Progress[edit source]
Chronic, in 20% improvement and fading of bearings.
Rheumatism nodosus[edit source]
Subcutaneous nodules affecting 20% of people with rheumatoid arthritis; histologically necrobiotic granulomas.
Etiology[edit source]
Most likely vascular changes and traumatization.
Clinical picture[edit source]
Multiple, subcutaneous, painful to touch nodules – typically over the elbows, knees, ulnar sides of the forearms and over the joints of the hands; nodes are rigid and movable.
Diagnosis[edit source]
Clinical picture + histology – necrobiosis = more extensive areas of degeneration of the coria collagen ligament, surrounded by histiocytes and giant cells.
Differential diagnosis[edit source]
Subcutaneous granuloma annulare is often difficult to differentiate, gouty nodules, mesenchymal tumors, acrodermatitis chronica atrophicans.
Therapy[edit source]
In most cases, intralesional application of corticoids is not necessary, if they are painful and limit movement, then surgical excision.
Progress[edit source]
Rheumatic nodules are permanent, causing difficulties in normal use of the hand.
Links[edit source]
References[edit source]
Jiří Štork et al. Dermatovenerology. Galen, Carolinum. 2008;
Presentation on the website http://kozni.lf1.cuni.cz;
Lectures by teachers at the Dermatovenerology Clinic of the 1st Faculty of Medicine, UK and VFN;
Jakub Holešovský, questions from dermatovenerology