Talk:Necrobiotic granulomatous processes

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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