Parthenon p.103, 2000
Cold urticaria
JAAD 53:373–388, 2005; The Clinical
Management of Itching. Parthenon p.103, 2000; J Clin Lab Med
74:902–910, 1969
Contact heat urticaria
JAAD 53:373–388, 2005
Cyclic edema
Drug reaction
JAAD 53:373–388, 2005
Eosinophilic myositis/perimyositis
JAAD 37:385–391, 1997
Episodic angioedema with eosinophilia
JAAD
53:373–388, 2005; Clin Exp Immunol 82:38–43, 1990;
NEJM 310:1621–1626, 1984
Estrogen-dependent inherited angioedema
J Allergy Clin
Immunol 106:546–550, 2000
Exercise-induced anaphylaxis, with or without food ingestion
JAAD 53:373–388, 2005
Familial Mediterranean fever
Fluid retention syndrome
Foods – peanuts, shellfish, milk, eggs, tree nuts, and foods
which cross-react with latex (kiwi, banana, avocado, chestnut)
JAAD 53:373–388, 2005
Gleich’s syndrome (episodic angioedema with eosinophilia) –
angioedema, urticaria, fever, periodic weight gain, eosinophilia,
increased IgM
AD 141:633–638, 2005; JAAD 20:21–27, 1989;
NEJM 310:1621–1626, 1984
Graves’ disease
JAAD 48:641–659, 2003
Henna (Lawsonia inermis)
Poster Session, European Academy
of Dermatology and Venereology, 2002
Hereditary angioedema – autosomal dominant; C’1 INH
deficiency
Medicine 71:206–215, 1992; type III – normal C1 INH
activity in women with relationship to estrogenic activity
JAAD
53:373–388, 2005; BJD 150:157–158, 2004; J Allergy Clin
Immunol 106:546–550, 2000; Lancet 356:213–217, 2000; NEJM
334:1666–1667, 1996; Am J Med 35:37–44, 1963; Am J Med Si
95:362–367, 1888
Hereditary angioedema with normal C’1 INH in women
JAAD
53:373–388, 2005
Hereditary vibratory angioedema
Hypereosinophilic syndrome
Medicine 54:1–27, 1975
Hypocomplementemic vasculitis
JAAD 48:311–340, 2003
Idiopathic hypereosinophilic syndrome
BJD 144:639, 2001;
Blood 83:2759–2779, 1994; AD 114:531–535, 1978
Insect venoms
JAAD 53:373–388, 2005
Leukemia – chronic lymphocytic leukemia
Ghatan p.122,
2002, Second Edition; acute lymphoblastic leukemia with
eosinophilia
Ped Derm 20:502–505, 2003
Leukotriene antagonist (monteleukast) administration
concurrently with aspirin
JAAD 53:373–388, 2005
Loiasis
Lupus erythematosus – systemic lupus erythematosus
JAAD
7:255–264, 1982
Monoclonal gammopathy
Ghatan p.122, 2002, Second Edition
Myeloma
Ghatan p.170, 2002, Second Edition
Necrobiotic xanthogranuloma with paraproteinemia –
antibody-mediated decreased levels of C1 esterase inhibitor
Hautarzt 45:339–343, 1994
NSAID (including aspirin)-induced angioedema
JAAD
53:373–388, 2005
Parvovirus B19 – neonatal angioedema due to
intrauterine infection with Parvovirus B19
BJD
143:428–430, 2000
Recurrent cutaneous necrotizing eosinophilic vasculitis
AD
130:1159–66, 1994
Radiocontrast media
JAAD 53:373–388, 2005
Serum sickness
Solar urticaria
JAAD 53:373–388, 2005
Superior vena cava syndrome
Urticaria
Rook p.2116–2117, 1998, Sixth Edition
Urticarial vasculitis
JAAD 49:S283–285, 2003; Clin Rev
Allergy Immunol 23:201–216, 2002; JAAD 38:899–905, 1998;
JAAD 38:899–905, 1998; Medicine 74:24–41, 1995; JAAD
26:441–448, 1992
Vibratory angioedema
JAAD 53:373–388, 2005
Waldenström’s macroglobulinemia
Ghatan p.122, 2002,
Second Edition
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