Skin Vascular Anatomy and Vasculitis
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Questions and Answers

What is a common clinical manifestation associated with IgA vasculitis?

  • Persistent headaches
  • Chronic joint pain
  • Palpable purpura not related to thrombocytopenia (correct)
  • Severe skin ulceration
  • Which type of cryoglobulinemic vasculitis is characterized by Raynaud’s phenomenon in about 30% of patients?

  • Type I cryoglobulinemia (correct)
  • Primary cryoglobulinemic vasculitis
  • Mixed cryoglobulinemic vasculitis
  • Type II cryoglobulinemia
  • What histological feature is observed in IgA vasculitis?

  • Leukocytoclastic vasculitis (correct)
  • Eosinophilic infiltration
  • Presence of cell necrosis
  • Granuloma formation
  • What is the typical age demographic for patients with IgA vasculitis?

    <p>Children under 20 years</p> Signup and view all the answers

    What does the direct immunofluorescence test reveal in IgA vasculitis?

    <p>Predominant IgA deposits</p> Signup and view all the answers

    Which disorders are associated with Churg-Strauss granulomas?

    <p>Systemic lupus erythematosus</p> Signup and view all the answers

    Which type of vasculitis is classified as a hypersensitivity vasculitis?

    <p>Cutaneous leukocytoclastic angiitis</p> Signup and view all the answers

    What distinguishes deep dermal necrobiosis in vasculitis cases?

    <p>Foci affecting collagen bundles surrounded by histiocytes</p> Signup and view all the answers

    Which of the following is associated with Microscopic Polyangiitis?

    <p>Necrotizing glomerulonephritis</p> Signup and view all the answers

    What percentage of cases for Microscopic Polyangiitis show positive ANCA?

    <p>80%</p> Signup and view all the answers

    Which clinical manifestation is NOT typically associated with Eosinophilic Granulomatosis with Polyangiitis?

    <p>Renal failure</p> Signup and view all the answers

    In which demographic is Macular Lymphocytic Arteritis (MLA) most commonly observed?

    <p>Women aged 40 years</p> Signup and view all the answers

    Which of the following symptoms is characteristic of Eosinophilic Granulomatosis with Polyangiitis?

    <p>Pulmonary infiltrates</p> Signup and view all the answers

    What is a common skin manifestation observed in Eosinophilic Granulomatosis with Polyangiitis?

    <p>Purpura</p> Signup and view all the answers

    Which of the following conditions is triggered by mycobacterial infection?

    <p>Microscopic Polyangiitis</p> Signup and view all the answers

    What type of lesions are typical of Eosinophilic Granulomatosis with Polyangiitis in terms of location?

    <p>Lower limbs</p> Signup and view all the answers

    What is a common presenting sign of Escherichia coli sepsis in newborns?

    <p>Livedo reticularis</p> Signup and view all the answers

    Which of the following conditions is related to neutrophilic vasculitis syndromes?

    <p>Cryoglobulinaemia</p> Signup and view all the answers

    Amantadine is linked to which dermatological condition?

    <p>Livedo reticularis</p> Signup and view all the answers

    What condition was observed in a case involving gemcitabine?

    <p>Livedo racemosa</p> Signup and view all the answers

    What significant clinical feature is discussed in relation to 64 cases of cryoglobulinaemia?

    <p>Biological characteristics</p> Signup and view all the answers

    Nicolau syndrome can be caused by which of the following medications?

    <p>Diclofenac sodium</p> Signup and view all the answers

    In the context of antineutrophil cytoplasmic antibody-associated vasculitis, which condition is highlighted?

    <p>Neutrophilic dermatoses</p> Signup and view all the answers

    Which of the following studies involves clinical findings in association with vasculitis?

    <p>Stephanie et al. on cryoglobulinaemia</p> Signup and view all the answers

    What criteria did the American College of Rheumatology establish in 1990 regarding giant cell arteritis?

    <p>They published diagnostic criteria for the classification.</p> Signup and view all the answers

    Which condition was specifically classified by the American College of Rheumatology in 1990 aside from giant cell arteritis?

    <p>Henoch-Schönlein purpura</p> Signup and view all the answers

    Which of the following authors published work on hypersensitivity vasculitis in 1990?

    <p>Calabrese LH</p> Signup and view all the answers

    In which publication can the 1990 criteria for the classification of henoch-Schönlein purpura be found?

    <p>Arthritis Rheumatism</p> Signup and view all the answers

    What skin condition was investigated in a two-year-old child due to pellagra?

    <p>Livedo reticularis</p> Signup and view all the answers

    What treatment showed a prompt response in a reported case of Susac syndrome with dermatological findings?

    <p>Intravenous immunoglobulin, steroids, and rituximab</p> Signup and view all the answers

    Which authors collaborated on the criteria for Henoch-Schönlein purpura classification in 1990?

    <p>All of the above</p> Signup and view all the answers

    What is the main focus of the classification criteria established by the American College of Rheumatology in 1990?

    <p>Diagnostic classification of vasculitis conditions</p> Signup and view all the answers

    What term describes the cone-shaped zone formed by nourishing arteries of the skin?

    <p>Cutaneous functional vascular unit</p> Signup and view all the answers

    Where are the nourishing arteries of the skin located?

    <p>In the hypodermis</p> Signup and view all the answers

    Which vascular plexus is also referred to as the cutaneous plexus?

    <p>Deep plexus</p> Signup and view all the answers

    What clinical aspect can be explained by the obstruction of the nourishing artery?

    <p>Livedo</p> Signup and view all the answers

    What describes the arrangement of arterioles and venules in the superficial dermis?

    <p>Superficial or subpapillary plexus</p> Signup and view all the answers

    What is a key finding for diagnosing cutaneous vasculitis?

    <p>Type of inflammatory infiltrate</p> Signup and view all the answers

    Which anatomical structures are primarily irrigated by the branches of the deep plexus?

    <p>Adipose tissue and deep dermis</p> Signup and view all the answers

    How do arterioles from the superficial plexus interact with the dermal papillae?

    <p>They ascend towards the dermal papillae</p> Signup and view all the answers

    Study Notes

    Skin Vascular Anatomy

    • Two interconnected plexuses: a deep and a superficial plexus.
    • Deep plexus (cutaneous plexus) located at the dermohypodermic junction; nourishes the hypodermis, deep dermis, and structures like hair follicles and glands.
    • Superficial (subpapillary) plexus in the superficial dermis; arterioles ascend to the dermal papillae and descend.
    • Cutaneous functional vascular unit: cone-shaped zone from epidermis surface to nourishing artery at the dermohypodermic junction. Obstruction of the nourishing artery (e.g., in livedo) causes venous stasis, creating a reticulated appearance.

    Cutaneous Vasculitis: Histologic Features

    • Inflammatory Infiltrate: A key diagnostic feature.
    • Deep dermal necrobiosis: foci affecting collagen bundles, surrounded by histiocytes in rosettes; associated with conditions like GEPA, MPA, rheumatoid arthritis, lupus, and adult-onset Still's disease.

    Cutaneous Vasculitis: Specific Types

    • Cutaneous Leukocytoclastic Angiitis (Hypersensitivity Vasculitis): Individualized in CHCC 1994 and CHCC 2012; classified as single-organ vasculitis.
    • Microscopic Polyangiitis: Segmental and focal necrotizing glomerulonephritis, extracapillary proliferation, no extra-vascular granuloma; ANCA positive in over 80% of cases (anti-myeloperoxidase). Associated with glomerulonephritis, neuropathy, hemorrhage, and gastrointestinal issues.
    • IgA Vasculitis: 87% accuracy in classification with criteria including palpable purpura (excluding thrombocytopenia), post-prandial abdominal pain, bloody diarrhea, GI hemorrhage, hematuria, age <20, and absence of precipitating drugs. Histologically non-specific leukocytoclastic vasculitis, but direct immunofluorescence shows predominant IgA deposits (though not specific). May present with atrophie blanche, Raynaud's, and inflammatory plaques/nodules.
    • Macular Lymphocytic Arteritis (MLA): Macular and pigmented rash, lymphocytic arteritis in the hypodermis/deep dermis; no destruction/necrosis. Affects lower limbs predominantly, women (70-80%), median age 40.
    • Eosinophilic Granulomatosis with Polyangiitis (EGPA): Necrotizing vasculitis, asthma, blood and tissue eosinophilia, systemic vasculitis; manifestations include mononeuropathy/polyneuropathy, pulmonary infiltrates, sino-nasal abnormalities, cardiomyopathy and cutaneous purpura, nodules, and urticaria (up to 50% of patients).

    Livedo Reticularis

    • Can be caused by various factors including infection (bacterial, viral, mycobacterial), inflammatory bowel disease, or drugs (e.g., minocycline, amantadine, norepinephrine). Also linked to conditions like pellagra, sarcoidosis, and Escherichia Coli sepsis. Associated with cryoglobulinemia.

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    Description

    Explore the complexities of skin vascular anatomy and the histological features of cutaneous vasculitis. This quiz covers the anatomical structures, pathological conditions, and specific types of cutaneous vasculitis you need to know for a deeper understanding of dermatological health.

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