מחלת שמברג
Benign dermatoses with pupura
נבדק על ידי Dr Philippa Vincent, MRCGPעודכן לאחרונה על ידי Dr Toni Hazell, FRCGPעודכן לאחרונה 15 אפריל 2026
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אנשי מקצוע רפואיים
מאמרי עיון מקצועיים מיועדים לשימוש של אנשי מקצוע בתחום הבריאות. הם נכתבים על ידי רופאים מבריטניה ומבוססים על ראיות מחקריות, הנחיות בריטיות ואירופאיות. ייתכן שתמצא אחד מהמאמרים שלנו מאמרי הבריאות יותר שימושי.
What is Schamberg's disease?
Synonyms: progressive pigmented purpuric dermatitis, Gougerot-Blum capillaritis, itching purpura, pigmented purpuric eruption1
Schamberg's disease is the most common type of the pigmented purpuric dermatoses (PPDs). It is chronic, benign, cutaneous eruptions characterised by petechiae, purpura and increased skin pigmentation (brown, red, or yellow patchy). The PPDs are grouped into:
Progressive pigmentary purpura or Schamberg's disease.
Pigmented purpuric lichenoid dermatitis of Gougerot and Blum - red/brown papules and plaques in men - which responds to psoralen combined with ultraviolet A (PUVA) treatment.
Purpura annularis telangiectodes - rare, with a preponderance in young females and manifesting as annular erythematous plaques and patches.
Eczematoid-like purpura of Doucas and Kapetanakis - occurring in men, with bilateral intensely itchy lesions on legs.
Lichen aureus - a localised persistent form of pigmented purpuric dermatitis.
Itching purpura of Lowenthal (disseminated pruriginous angiodermatitis) - rare (like Schamberg's disease) but accompanied by itching.
There is clinical and histological overlap between these and they may actually represent variable presentations of the same disease process.
Who is affected by Schamberg disease? (Epidemiology)
Schamberg's disease is rare and there are few epidemiological studies in the literature.
Schamberg disease may affect all ages but commonly occurs in middle-aged to older men and less frequently in children, although cases have been reported in children aged under two. 2
There has been a case report of four family members with Schamberg's disease, suggesting a possible genetic link.3
Schamberg's disease causes (aetiology) 4
The underlying cause is not known. However, the following have been postulated:
Recent viral infection.
צריכת אלכוהול.
Hypersensitivity to an unknown causal agent.
Aberrant cell-mediated immunity (perivascular infiltrate has specific types of CD cells only).
Associated with certain medications - thiamine, aspirin, chlordiazepoxide and paracetamol. It has also been reported with bezafibrate and amlodipine.5
There is an association with hepatitis B, in which case treatment of the hepatitis may improve the skin.
Schamberg's disease symptoms4
There are no symptoms of Schamberg's disease apart from itching and patients noting their skin looks blotchy. For some this is enough to cause psychological distress. However, some patients have reported pains in their limbs - which may be coincidental.
Lesions are most commonly on the lower limbs bilaterally but can occur anywhere or be unilateral. A case involving the genitals has been reported.
The lesions consist of:
Asymmetrical brown/orange patches.
Non-blanchable purpura.
Petechiae called 'cayenne pepper spots' (develop at the edge of old lesions).
Patterns can vary - for example, annular, linear. There may also be associated lichenification, scaling and pruritic marks.
אבחנה מבדלת16
Other causes of pigmented purpura include:
וסקוליטיס - for example, leukocytoclastic vasculitis.
לימפומה של תאי T (especially if presenting in young males).
Trauma.
Self-induced purpura or non-accidental injury to a child.
Purpura annularis telangioectodes (Majocci disease).
Primary benign hypergammaglobulinaemic purpura of Waldenström.8
חקירות
Blood tests - including platelets and clotting - are usually normal.
Autoantibody screen and hepatitis serology should be performed.
Skin biopsy - histology reveals a capillaritis of dermal vessels. Other changes that may be seen include perivascular inflammatory infiltrate, endothelial hypertrophy with extravasation of blood cells and haemosiderin-laden macrophages.9
Examination of the skin, using a dermatoscope, may be helpful although there are limited reports in the literature.110
מחלות נלוות11 12
הפרעות בבלוטת התריס.
Hepatic disease, including hepatitis B.
ממאירויות.
Dyslipidaemias.
Schamberg's disease treatment and management1 4 11
Any suspected precipitants should be withdrawn.
Pruritis - treat with mild topical corticosteroid or antihistamines.
Good results have been obtained with narrow-band ultraviolet light.
Aminaphtone, a drug normally used in other venous conditions such as chronic venous congestion of the lower limbs can be used.13
Superimposed infection - will need antibiotics.
Systemic steroids provide some benefits but these are outweighed by the risks of systemic side-effects.
Advanced fluorescent technology using pulses of light has produced some promising cosmetic results.1415
Other tried treatments include vitamin C supplements, laser therapy and wearing support hosiery to prevent venous stasis. There is no evidence from randomised blinded trials of definite benefit of the former two, although case studies exist suggesting benefits from both. Immunosuppressants have also been used. PUVA treatment has been used successfully.2
תחזית
Schamberg's disease usually runs a chronic course with frequent exacerbations and remissions. The rash may be present for many years with slow extension. Pigmented purpura may occasionally disappear spontaneously.
The development of T-cell lymphoma in patients with Schamberg's disease has been reported.16
עדכונים בלעדיים לאנשי מקצוע בתחום הבריאות
הישאר מעודכן עם העדכונים הקליניים האחרונים, תובנות מקצועיות והנחיות מבוססות ראיות. הניוזלטר של Patient Pro אוסף תוכן חיוני לאנשי מקצוע בתחום הבריאות - נשלח ישירות לתיבת הדואר הנכנס שלך.
על ידי הרשמה אתה מקבל את שלנו מדיניות הפרטיות שלנו. באפשרותך לבטל את המנוי בכל עת. לעולם לא נמכור את הנתונים שלך.
קריאה נוספת והפניות
- Zaldivar Fujigaki JL, Anjum F; Schamberg Disease. StatPearls, Jan 2026
- Spigariolo CB, Giacalone S, Nazzaro G; Pigmented Purpuric Dermatoses: A Complete Narrative Review. J Clin Med. 2021 May 25;10(11). pii: jcm10112283. doi: 10.3390/jcm10112283.
- Sethuraman G, Sugandhan S, Bansal A ואחרים; מחלות עור משפחתיות מסוג פורפורה פיגמנטרית. J Dermatol. ספטמבר 2006;33(9):639–41.
- קפילריטיס; DermNet NZ
- Schetz D, Kocic I; A new adverse drug reaction - Schamberg's disease caused by amlodipine administration - a case report. Br J Clin Pharmacol. 2015 Aug 10. doi: 10.1111/bcp.12742.
- Ho C, Yan P, Mistry N, et al; Dermacase: Can you identify this condition? 4. Progressive pigmented purpuric Can Fam Physician. 2010 Oct;56(10):1023, 1024-5.
- Ugajin T, Satoh T, Yokozeki H, et al; Mycosis fungoides presenting as pigmented purpuric eruption. Eur J Dermatol. 2005 Nov-Dec;15(6):489-91.
- Nikam BP, Singh NJ, Shetty DD; Primary benign hypergammaglobulinemic purpura of Waldenstrom masquerading as disseminated Schamberg's purpura. Indian J Dermatol Venereol Leprol. 2011 Mar-Apr;77(2):205-8.
- Billings S et al; Inflammatory Dermatopathology: A Pathologist's Survival Guide, 2010.
- Khopkar U; Dermoscopy and Trichoscopy in Diseases of the Brown Skin, 2013.
- Kim DH, Seo SH, Ahn HH, et al; Characteristics and Clinical Manifestations of Pigmented Purpuric Dermatosis. Ann Dermatol. 2015 Aug;27(4):404-10. doi: 10.5021/ad.2015.27.4.404. Epub 2015 Jul 29.
- Sardana K, Sarkar R, Sehgal VN; דרמטוזות פורפוריות פיגמנטריות: סקירה כללית; Int J Dermatol. 2004 Jul;43(7):482-8.
- de Godoy JM, Batigalia F; Aminaphtone in the control of Schamberg's disease. Thromb J. 2009 Jun 11;7:8.
- Manolakos DA, Weiss J, Glick B, et al; טיפול במחלת שַמְבֶּרְג באמצעות טכנולוגיית פלואורסצנציה מתקדמת. J Drugs Dermatol. אפריל 2012;11(4):528-9.
- Demidion DV, Olisova OY, Kostenko AY, et al; Complete clearance of Schamberg disease lesions with intense pulsed light. Photodermatol Photoimmunol Photomed. 2023 Jan;39(1):78-81. doi: 10.1111/phpp.12810. Epub 2022 Jun 14.
- Shen A ואח׳; Capillaritis as a potential harbinger of cutaneous T-cell lymphoma, 2004
אודות המבקרצפה בפרופיל המלא

Dr Philippa Vincent, MRCGP
רופא כללי, מחבר רפואי
MB BS, Bsc, MRCGP (2000), DCH, DFSRH, DRCOG
ד"ר Philippa וינסנט הוא רופא משפחה ב-NHS העובד בצפון לונדון.
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