Differentials

Necrotizing fasciitis

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Initial findings are nonspecific and can be similar to those of cellulitis.

Marked pain, often out of proportion to the exam, and necrotic bullous change are clinical clues.

Crepitus may be present as a late finding if a mixed anaerobic etiology is responsible.

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Surgical exploration is definitive for diagnosis and a requirement for treatment. This is limb- and potentially life-threatening, and surgical consultation should not be delayed if necrotizing fasciitis is suspected. MRI is helpful if the diagnosis is in doubt.[47][48]

MRI: contrast enhancement, thickening of deep fasciae with fluid collection.

Thrombophlebitis, superficial

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Tender, palpable cord along affected vein often present.

Presence or recent presence of intravenous catheter or needle also suggests this diagnosis.

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Clinical diagnosis.

Deep vein thrombosis

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Tenderness of involved vein, history of prior deep vein thrombosis, prolonged immobility, or hypercoagulable state.

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Duplex ultrasonography: presence of a thrombus within the vein.

Gout

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Suspected in those with history of gout or if area of skin involvement is closely associated with a joint, particularly the first metatarsophalangeal or knee joint.

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Presence of urate crystals in joint aspirate.

Lyme disease

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Also known as erythema migrans.

Residence in or travel to endemic area, history of tick exposure, involvement of sites that are unusual for bacterial cellulitis (e.g., axilla, popliteal fossa, or abdomen) are suggestive.[49]

Sometimes has an area of central clearing within the erythema.

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May be differentiated clinically. Serologic testing for Borrelia burgdorferi.[50][51]

Dermatitis, contact

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Well-demarcated skin involvement, pruritus, and exposure history are suggestive.[52]

Often diagnosed on clinical grounds alone.

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Biopsy: intraepidermal spongiosis with monocyte and histiocyte dermal infiltration suggest an allergic contact dermatitis. Irritant dermatitis is characterized by superficial vesicles containing polymorphonuclear leukocytes.[53]

Insect bites and stings

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History of insect exposure and pruritus. Often diagnosed on clinical grounds alone.

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Biopsy: wedge-shaped dermal mixed inflammatory infiltrate is characteristic. Eosinophils often predominate.[53]

Fixed drug reactions

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History of similar reaction with prior exposure to same drug; well-demarcated round or oval area of involvement; itching, burning; involvement of lips and/or genitalia.

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Clinical diagnosis.

Eosinophilic cellulitis (Wells syndrome)

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A short prodrome of itching and burning may precede onset of single or multiple lesions. Recurrence is common and resolution of each episode may occur over weeks.[54]

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Histopathology: dermal infiltration with eosinophils and a peripheral eosinophilia can be seen as well.[54]

Sweet syndrome

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Well-defined erythematous plaques with a mammillated surface are typical.

Fever, malaise, myalgias, and arthralgias are common.[55]

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Histopathology: dermal infiltration by polymorphonuclear leukocytes.[55]

Inflammatory carcinoma (carcinoma erysipeloides)

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Involvement of breast, absence of fever.

This represents an advanced form of cancer.

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Mammography and biopsy should not be delayed.

Relapsing polychondritis

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Bilateral involvement, particularly of auricular (pinnae spared) or nasal cartilage, history of similar reaction.[56]

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Clinical diagnosis.

Calciphylaxis

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Painful, retiform lesions, often below the knee, with palpable characteristic subcutaneous plaques. Subsequent ulceration may develop. Seen most often in patients with end stage renal disease.[57]

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Diagnosis is often made clinically, especially with evolution of lesions. Biopsy is generally avoided due to concern over poor subsequent healing.[57]

Lipodermatosclerosis

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Associated with middle-aged women, especially those with venous insufficiency. Seeming predilection for medial leg.[58]

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A clinical diagnosis often suffices. Biopsy has been associated with development of chronic ulceration.[58]

Familial Mediterranean fever

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A positive family history, recurrent episodes, association with syndrome of fever, serositis, and lower extremity involvement with erysipelas-like lesions are suggestive.[52]

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Clinical diagnosis.

Lymphedema

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History of malignancy, previous surgery, radiation therapy, travel to endemic filariasis area, or family history of lymphedema. Painless unilateral swelling of extremity; non-pitting edema; skin changes. Symptoms of limb heaviness or weakness.

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Lymphoscintigram: dermal backflow, delayed or absent transport, or lack of visualization of lymph nodes.

MRI or CT scan of affected extremity: thickened skin; honeycombing of fluid and fibrous tissue above the muscle fascia.

Ultrasound of affected area: thickening of epifascial compartment and skin.

Lymphangiography: location of a specific anatomic obstruction.

Blood smear for filariasis: presence of microfilariae.

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