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Histopathology
Septal Prototype Miescher's septal micro-granulomas (M) Greater Septal Thickening Prominent Granulomata Septal Lymphoplasmacytic infiltrate Septal Neutrophils splayed b/t collagen in reticular dermis
Clinical Pathophysiology - Treatment Bruise-like; Fever, arthritis, malaise TH1 idiopathic >infxn (Strep) > sarcoid, IBD, OCPs, coccidio Tx: bed rest, salicylates or NSAID, SSKI
Nodules migrate or undergo centrifugal spread w/ central clearing Idiopathic (occ. Strep or Thyroid disease); Chronic course. Tx: SSKI (clears in weeks) Dermal & subcut. Sclerosis; Heal w/ hyperpigmentation & atrophy; No systemic sx Ulceration & oily discharge (like pancreatic pann); Tx: Doxy or Dapsone; EtOH PiMM (nl); PiMZ (heterozygote w/ moderate dz); PiZZ (homozygous, severe dz) Associated w/ emphysema, hepatitis, cirrhosis, vasculitis, angioedema, psoriasis.
Clinical Pathophysiology - Treatment Tender nodules ulceration & drainage Slowly healing lipoatrophic scars Erythema Induratum assoc. w/ tuberculosis; Others: Nocardia, drugs (PTU)
Subcutaneous nodules pain; migrate; oily discharge Pancreatic Acinar Cell carcinoma (#1) > pancreatitis, other panc. Ca. enzymes (LIPASE has clearest relationship), trypsin, amylase; Octreotide to panc enzymes; Schmids triad: nodular lesions, polyarthritis, eosinophilia (poor prognosis) Skin is cold, rigid, board-like (sparing of palms, soles, genitals) Associate w/ serious illness (75% of cases fatal, usually septicemia) Kid fat has saturated FAs (melting pt), so crystal more likely to deposit. Type A (microsize) crystals are (but found in normal infants <6mos) Hypercalcemia, thrombocytopenia > gest. DM, Rh mismatch, meconium Type B (larger) crystals arranged in rosettes elicits granulomatous response Good progrnosis. Rare complication of systemic high dose Rapid Corticosteroid Withdrawl Type B (larger) crystals arranged in rosettes elicits granulomatous response Tender nodules 33% have DLE; 10% have SLE; Rare; Indurated painful plaques with ulceration & lipoatrophy Tx dermatomyositis: prednisone, MTX, azathioprine, cyclosporine A, IVIG
mid age, elderly premature 1st week of life Newborn Infants 20-60
Sclerema neonatorum Subcutaneous fat necrosis of the newborn Post-steroid panniculitis Lupus Panniculitis Lupus Profundus Subcutaneous LE Dermatomyositis Panniculitis Traumatic Panniculitis Cold panniculitis Sclerosing lipogranuloma Injectable (Texiers disease) Blunt trauma Lipodermatosclerosis Sclerosing Panniculitis Hypodermitis sclerodermiformis Infectious Panniculitis Cytophagic Histiocytic Pann. Panniculitis-like subcutaneous lymphoma w/ cytophagocytosis
Buttocks & Thighs Proximal Extremity Cheeks, arms, trunk Shawl, cheeks Butt, abdomen, thighs, arms
Cold panniculitis - erythematous, firm nodules @ cheeks and chin (infants & young women equestrians) Sclerosing lipogranuloma - granulomatous nodules 2 self-inject oily materials (genitalia of young males) Injectable (Texiers disease) - sclerotic lesions w/ lilac borders @ buttocks & thighs 2 vit. K injections (with distribution of 'cowboy gunbelt and holster'. Blunt trauma - granuloma w/ foreign body present (esp breasts, LEs, hands & arms) Distal malleolar LEs Old fatties F>M Clinical: venous stasis heals with atrophy & sclerosis Tx: stanozolol, compression. Oxandrolone, U/S, pentoxifylline, phlebectomy. Clinical: lfluctuant nodules that ulcerate and drain Pathogens: bacteria, mycobacteria, fungi (dermatophytes, atypicals, Candida). Tx: Abx; Surgery for grain-forming bacteria/fungi (mycetoma, botryomycosis) Clinical: Subcutan nodules, fever, HSM, pancytopenia, liver failure, DIC, bleeds. Assn: Lymphoma (esp subcutaneous panniculitis-like T-cell lymphoma) Also consider malignant subcutaneous infiltrates (T-cell lymphoma)