Dermatologic Differential Diagnosis.pdf. - Famona Site

384 A CLINICIAN’S GUIDE TO DERMATOLOGIC DIFFERENTIAL DIAGNOSIS, VOLUME 1
Nodular subepidermal fibroma Cutis 69:173–174, 2002
Peripheral neuroepithelioma Curr Prob Derm 14:41–70, 2002
Pilar cyst
Pilomatrixoma Cutis 69:173–174, 2002
Plasmacytoma – extramedullary plasmacytoma – violaceous
brown nodule JAAD 49:S255–258, 2003; primary
plasmacytoma JAAD 38:820–834, 1998
Plasmacytosis, systemic JAAD 38:629–631, 1998
Porocarcinoma AD 136:1409–1414, 2000
Post-transplantation lymphoproliferative disorder JAAD
52:S123–124, 2005; AD 140:1140–1164, 2004; JAAD
51:778–780, 2004
Progressive eruptive histiocytomas (brown) JAAD 35:323–325,
1996
Rhabdomyosarcoma
Soft tissue sarcoma
Squamous cell carcinoma – complicating venous stasis ulcers
South Med J 58:779–781, 1965
Subcutaneous myeloid sarcoma AD 141:104–106, 2005
PARANEOPLASTIC DISEASES
Eosinophilic dermatosis of myeloproliferative disease – face,
scalp; scaly red nodules; trunk – red nodules; extremities – red
nodules and hemorrhagic papules AD 137:1378–1380, 2001
Erythema nodosum associated with acute myelogenous
leukemia, chronic myelogenous leukemia, chronic
myelomonocytic leukemia Bolognia p.1947, 2003
Exaggerated arthropod bite reactions – chronic lymphocytic
leukemia Bolognia p.1947, 2003
Necrobiotic xanthogranuloma with paraproteinemia Medicine
(Baltimore) 65:376–388, 1986
Neutrophilic panniculitis associated with myelodysplastic
syndrome JAAD 50:280–285, 2004
Pancreatic panniculitis – pancreatic carcinoma
Paraneoplastic septal panniculitis associated with acute
myelogenous leukemia BJD 144:905–906, 2001
Paraneoplastic vasculitis – nodules, panniculitis J Rheumatol
18:721–727, 1991
Polyarteritis nodosa – associated with hairy cell leukemia, and
chronic myelomonocytic leukemia Bolognia p.1947, 2003
Thrombophlebitis migrans (Trousseau’s sign) – association with
internal malignancy Circulation 22:780, 1960
PRIMARY CUTANEOUS DISEASE
Anetoderma of Jadassohn AD 102:697–698, 1970
Epidermolysis bullosa pruriginosa – domnant dystrophic or
recessive dystrophic; mild acral blistering at birth or early
childhood; violaceous papular and nodular lesions in linear
array on shins, forearms, trunk; lichenified hypertrophic and
verrucous plaques in adults, reticulate scarring, dermatitis with
lichenified plaques, violaceous linear scars, albopapuloid
lesions of the trunk, prurigo nodularis-like lesions, milia BJD
152:1332–1334, 2005; BJD 146:267–274, 2002;
BJD 130:617–625, 1994
Erythema elevatum diutinum Cutis 68:41–42, 55, 2001;
Cutis 34:41–43, 1984
Granuloma annulare
Keratosis lichenoides chronica – extremities and buttocks
JAAD 38:306–309, 1998; JAAD 37:263–264, 1997;
AD 131:609–614, 1995; AD 105:739–743, 1972
Nodular erythrocyanosis – calves, knees, thighs, buttocks of
women with paralysis Rook p.2204,2206–2207, 1998,
Sixth Edition
Prurigo nodularis – idiopathic or associated with lymphoma,
peripheral T-cell lymphoma (Lennert’s lymphoma)
Cutis 51:355–358, 1993; Hodgkin’s disease Dermatologica
182:243–246, 1991; Ped Derm 7:136–139, 1990; gluten
sensitive enteropathy BJD 95:89–92, 1976; AIDS
JAAD 33:837–838, 1995; uremia South Med J 68:138–141,
1975; depression, liver disease, α-1 antitrypsin deficiency
Australas J Dermatol 32:151–157, 1991; malabsorption
Dermatologica 169:211–214, 1984
PSYCHOCUTANEOUS DISEASES
Factitial panniculitis Rook p.2204,2801, 1998, Sixth Edition
SYNDROMES
Behçet’s disease – erythema nodosum-like lesions
BJD 147:331–336, 2002; JAAD 40:1–18, 1999;
JAAD 36:689–696, 1997; Ped Derm 11:95–101, 1995;
subcutaneous red nodules (vasculitis) JAAD 31:493–495,
1994; Behçet’s disease JAAD 41:540–545, 1999;
NEJM 341:1284–1290, 1999; neutrophilic eccrine hidradenitis
Cutis 68:107–111, 2001
Congenital self-healing reticulohistiocytosis –
Hashimoto–Pritzker type AD 134:625–630, 1998
Disseminated lipogranulomatosis (Farber’s disease)
Familial Mediterranean fever – panniculitis AD 134:929–931,
1998; erythema nodosum-like lesions AD 112:364–366, 1976
Fibrodysplasia ossificans progressiva
Hemophagocytic syndrome AD 128:193–200, 1992
Hypereosinophilic syndrome AD 132:535–541, 1996; Medicine
54:1–27, 1975
Hyper-IgD syndrome – red macules or papules, urticaria,
red nodules, combinations of fever, arthritis, and rash, annular
erythema, and pustules – autosomal recessive; mevalonate
kinase deficiency AD 136:1487–1494, 2000; AD 130:59–65,
1994
Hyper-IgM syndrome – X-linked; sarcoid-like granulomas;
multiple papulonodules of face, buttocks, arms Ped Derm
21:39–43, 2004
Nakajo syndrome – nodular erythema with digital changes
Neurofibromatosis type 1
Relapsing polychondritis – panniculitis Dermatology
193:266–268, 1996
Sweet’s syndrome JAAD 31:535–536, 1994; septal erythema
nodosum-like panniculitis AD 121:785–788, 1985; subcutaneous
Sweet’s syndrome AD 138:1551–1554, 2002
TRAUMA
Cold panniculitis, including equestrian cold panniculitis in
women AD 116:1025–1027, 1980
Hematoma – palpable painful mass of thigh
Intravenous drug abuse (IVDA) – tracks
VASCULAR DISEASES
Angiokeratoma circumscriptum Ghatan p.73, 2002, Second
Edition
Angiosarcoma – purple nodules BJD 138:692–694, 1998;
AD 124:263–264, 266–267, 1988