DermKnowledgeBASE: Cryoglobulinemic Purpura

Cryoglobulinemic Purpura

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The text is the summary of recent articles on Cryoglobulinemic Purpura at 75 thresold from National Library of Medicine (NLM). This information is subject to NCBI's Disclaimer and Copyright notice.

Examples are provided by hypocomplementemic urticarial vasculitis, cryoglobulinemic purpura, lymphocytic Vasculitis of livedoid lesions [1]. This paper describes the cutaneous histopathological findings of some Vasculitis related Pediatric diseases, be they pertaining to a Systemic Vasculitis with corresponding cutaneous Vasculitis, to a systemic Vasculitis with sporadic cutaneous vasculitic involvement, and to a systemic Vasculitis without cutaneous vasculitic involvement [2]. Type and level of histopathological vasculitic involvement, caliber of the vessel, type of vasculitis associated Infiltrate, are likewise reliable integration in the complex diagnostic path of Vasculitis in childhood [3]. In this article mixed cryoglobulinemia, type II, was diagnosed in a negative for hepatitis b or C patient suffering from visceral leishmaniasis [4]. Antimicrobial therapy against leishmania eliminated the cryoglobulin titer, as well as the clinical manifestations of cryoglobulinemia [5].

Since it is well known that commonly there is relatively dense Inflammatory cell Infiltration mainly in the upper Dermis in lichen planus, the same RT-PCR procedure was performed using RNA from peripheral blood leukocytes from the same patients [6]. The peculiarity of the case presented was its complication with left fibular nerve Neuropathy [7]. So called benign IgG or IgA monoclonal gammopathy may be associated with certain rare clinical entities such as mucinar papulosis or leakage syndrom [8]. When a lymphoplasmacytic disease can be excluded, hypogammaglobulinemia is usually genetic, although rare causes of acquired hypogammaglobulinemia exist [9]. Improvement of the stomatological signs of the disease was noted in all the patients: salivation increased, the parotid glands considerably decreased in size, parotiditis recurrences were absent or seldom, and the Number of the functioning salivary glands of the lower Lip increased [10].

The above therapy showed a positive effect on ophthalmological symptoms of the disease in 5 patients [11]. Combination therapy (6-MP and CP) was effective for the management of such Systemic symptoms of SD and SS as Arthritis, lymphadenopathy, hepatosplenomegaly, Exudative polyserositis, polyneuritis, ulcerative-necrotic Vasculitis, cerebrovasculitis, cryoglobulinemic purpura and glomerulonephritis [12]. Initially both C1q and C3 were depressed in two patients with SLE, one with cryoglobulinemic purpura and one with HbsAg-positive serum sickness, each with acute Vasculitis [13].

References: 1 , 2 , 3 , 4 , 5 , 6 , 7 , 8 , 9 , 10 , 11 , 12 , 13 ,

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About Me

I have varied research interests ranging from eHealth, Health Information Exchange, Clinical Trials and Research, Contact Dermatitis, Bioinformatics, and Cosmetic Dermatology. I have work experience in Canada as an eHealth analyst, and in Dubai and India as a Specialist Dermatologist.


Bell Raj Eapen
Hamilton, ON