Ischemic Dermatopathy Flashcards

1
Q

What is ischemic dermatopathy?

A

syndrome that results from loss of blood supply from either vasculitis or vasculopathy, “cell-poor vasculitis” (dermatopathologists)

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2
Q

Forms of ischemic dermatopathy

A

post-rabies vaccination scarring, alopecia, and dermatomyositis, similar histologic cell-poor vasculitis changes seen with familial German shepherd dog vasculopathy, some “lupoid” dermatoses, and the disease in greyhounds

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3
Q

Five forms of ischemic dermatopathy

A
  1. familial predisposed dermatomyositis
  2. juvenile-onset dermatomyositis in non familial recognized breeds
  3. post-rabies vaccination panniculitis
  4. generalized vaccine-induced ischemic dermatopathy
  5. adult-onset ischemic dermatopathy lesions with no temporal association with vaccines
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4
Q

Etiology of ischemic dermatopathy

A

vascular disease is relatively mild or more subtle in onset or severity, leading to tissue hypoxia; leading to follicular, dermal, and epidermal changes without the more typical vascular changes of hemorrhage, edema, and necrosis

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5
Q

Lesions of less severe ischemic dermatopathy

A

scarring alopecia, shiny scaly skin, and comedones

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6
Q

Vaccine-associated ischemic dermatopathy

A

2-8 months after vaccination, various combinations of plaques, nodules, alopecia, scale, erosions, ulcers, crusts, hyperpigmentation, and scarring

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7
Q

Locations of vaccine-associated ischemic dermatopathy

A

may occur at site of vaccination, pinnae (usually the apex and often the concave surface especially at pinnal margins), face, paw pads, tip of tail, periocular region, and over bony prominences, erosions and ulcers may be seen on the tongue; may have associated atrophic myopathy

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8
Q

Differentials for ischemic dermatopathy with linear vascular pattern with ecchymosis or petechia

A

coagulopathy, SLE, cold agglutinin disease, frost-bite, DIC, and lymphoreticular neoplasia

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9
Q

Differentials for ischemic dermatopathy with acute necrotic lesions and ulceration

A

sub epidermal bullous diseases, burns, deep pyoderma

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10
Q

Differentials for ischemic dermatopathy with predominantly urticarial lesions

A

hypersensitivity disorders not associated with vasculitis

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11
Q

Differentials for ischemic dermatopathy with early focal lesions

A

Demodex, dermatophytosis, DLE, dermatomyositis

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12
Q

Infectious diseases that can lead to vasculitis and ischemic dermatopathy

A

Babes, Echrlichia/Anaplasma, Bartonella, Rickettsia rickettsii, Borrelia burgdorferi, and Leishmania infantum; identification does not prove causation but would be suspicious and warrant therapy

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13
Q

Sources of septic vasculitis

A

deep pyoderma, cellulitis, bacterial endocarditis

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14
Q

Thrombus formation in ischemic dermatopathy

A

thrombus formation, fibrin in the thrombus is broken down, results in formation of D-dimers (fibrin degradation products); mAb based assay detects D-dimers in the blood: 15 dogs with vasculitis had thrombi present in skin biopsy and D-dimer levels greater than 500ng/mL (specificity 100%, sensitivity 64%), 11 dogs had no thrombi detected and variable D-dimer levels; fibrinogen levels elevated >normal/287mg/dL in all vasculitis dogs

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15
Q

IFA or IHC in vasculitis

A

not needed or useful for diagnosis bc best done within 4 hours of lesion formation and no later than 24 hours; may demonstrate immunoglobulin, complement, or both in vessel walls and occasionally at BMZ in both neutrophilic and lymphocytic forms of cutaneous vasculitis

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16
Q

Clinical course of vasculitis varies depending on syndrome and cause

A

single episode lasting a few weeks, or may be chronic and lifelong or recurrent; outcome depends on extent of organ involvement (particularly renal and neurologic) and underlying or precipitating factors; once immune complexes and immune system stimulation, even controlling the primary cause may not immediately resolve the vasculitis

17
Q

Treatment of ischemic dermatopathy

A

underlying or precipitating factor treatment + pentoxifylline, glucocorticoids with or without azathioprine, cyclosporine, in combination, Vitamin E as an adjunct, may be stopped after 4-6 months or continued lifelong

18
Q

Proliferative thrombovascular necrosis of the pinnae

A

slowly progressive and usually unresponsive to most medical therapies, though some respond to pentoxifylline, if that is ineffective tx of choice is partial surgical removal of the pinna, relapses more common when attempt to leave tissue

19
Q

Focal cutaneous vasculitis and alopecia subsequent to injections

A

may respond to pentoxifylline (up to 75% reduction in lesion size) or may be treated by complete surgical excision, or occasionally spontaneously resolve; topical tacrolimus can be effective in some cases, logical NOT to repeat the vaccine unless required by law due to possibility of repeat reactions

20
Q

Solar vasculopathy

A

minimize UV exposure (both UVB and UVA though UVB most likely the more problematic), keep pet indoors and minimize sun exposure through glass, use of sunscreen 30spf or greater with UVA blockers and solar-protective garments