Acquired ichthyosis




Input patient's signs and symptoms


Narrow down the case reports



Total: 50 (papers)

  


(per page)
Matched Phenotype  Gene  Mutation  MeSH
Rank
(Similarity)
PMID
(PMCID)
1
(35.3%)
19684985
Myelopathy and adult T-cell leukemia associated with HTLV-1 in a young patient with hearing loss as the initial manifestation of disease.
Goncalves DU, Felipe L, Carneiro-Proietti AB, Guedes AC, Martins-Filho OA, Lambertucci JR.
Rev Soc Bras Med Trop. 2009;42(3):336-7.
Facial palsy
Homo sapiens Male Tropical Spastic Paraparesis Young Adult
2
(28.9%)
19661032
Acquired ichthyosis as a paraneoplastic syndrome in Hodgkin's disease.
Riesco Martinez MC, Munoz Martin AJ, Zamberk Majlis P, Adeva Alfonso J, Sabin Dominguez P, Garcia Alfonso P, Perez Fernandez R.
Clin Transl Oncol. 2009;11(8):552-3.
Palmoplantar hyperkeratosis
Aged, 80 and over Hodgkin Disease Homo sapiens Ichthyoses Male Paraneoplastic Syndromes
2
(28.9%)
17409605
Acquired ichthyosis disclosing non-Hodgkin's malignant lymphoma.
Rabhi M, Ennibi K, Harket A, Al Bouzidi A, Labraimi A, Chaari J, Toloune F.
Intern Med. 2007;46(7):397-9.
Palmoplantar hyperkeratosis
Disease Progression Fatal Outcome Health Risk Assessment Homo sapiens Ichthyoses Immunohistochemistry Lymphoma, Non-Hodgkin Male Middle Aged Paraneoplastic Syndromes Severity of Illness Index X-Ray Computed Tomography
2
(28.9%)
11226897
[Paraneoplastic acquired ichthyosis revealing non-Hodgkin's lymphoma].
Estines O, Grosieux-Dauger C, Derancourt C, Patey M, Durlach A, Bernard P.
Ann Dermatol Venereol. 2001;128(1):31-4.
Palmoplantar hyperkeratosis
Homo sapiens Ichthyoses Lymphoma, Non-Hodgkin Male Middle Aged Paraneoplastic Syndromes
5
(27.8%)
7482067
[Systemic lupus erythematosus and antiphospholipid antibody syndrome in a patient with congenital ichthyosiform erythroderma].
Nishiyama S, Miyawaki S.
Ryumachi. 1995;35(4):688-92.
Proteinuria Gingival bleeding
APOH
Adult Antiphospholipid Syndrome Congenital Nonbullous Ichthyosiform Erythroderma Females Homo sapiens Lupus Erythematosus, Systemic Pregnancy
6
(17.5%)
24090894
[Dermatomyositis and acute interstitial lung disease associated with MDA-5 antibodies: an atypical case].
Girard C, Vincent T, Bessis D.
Ann Dermatol Venereol. 2013;140(10):628-34.
Skin rash Calcinosis
IFIH1
Acute Disease Adult Antibody Specificity Autoantibodies Autoantigens Calcinosis DEAD-box RNA Helicases Dermatomyositis Erythema Homo sapiens Ichthyoses Immunosuppressive Agents Interferon-Induced Helicase, IFIH1 Lung Diseases, Interstitial Male Skin Ulcer Smoking beta Thalassemia
6
(17.5%)
22515579
Hydroxyurea-induced dermatomyositis: true amyopathic dermatomyositis or dermatomyositis-like eruption?
Nofal A, El-Din ES.
Int J Dermatol. 2012;51(5):535-41.
Palmoplantar keratoderma Proximal muscle weakness
Antineoplastic Agents Dermatomyositis Drug Eruptions Females Homo sapiens Terminology as Topic Withholding Treatment
8
(4.0%)
29928199
(6006631)
Porphyria Cutanea Tarda Presenting with Scleroderma, Ichthyosis, Alopecia, and Vitiligo.
MacGillivray ME, Salopek TG.
Case Rep Dermatol. 2018;10(2):115-121.
Vitiligo
8
(4.0%)
29469781
Ponatinib-induced ichthyosiform drug eruption: insights into acquired ichthyosis.
Xu H, Busam KJ, Mauro MJ, Markova A.
Dermatol Online J. 2017;23(10):.
Leukemia
Antineoplastic Agents Drug Eruptions Homo sapiens Ichthyoses Imidazoles Male Precursor Cell Lymphoblastic Leukemia Lymphoma Protein Kinase Inhibitors Pyridazines
8
(4.0%)
25838865
(4377237)
Multiple paraneoplastic syndromes revealing non-small cell lung carcinoma.
Youssef M, Kechida M, Cheikhmohamed S, Moussa A.
Pan Afr Med J. 2014;19:237.
Erythroderma
Homo sapiens Lung Neoplasms Male Middle Aged Paraneoplastic Syndromes Pneumonectomy X-Ray Computed Tomography
        

Phenotype(s) retrieved from Orphanet

    Total: 15

HPO ID Term Frequency
HP:0000958 Dry skin Very frequent (99-80%)
HP:0000989 Pruritus Very frequent (99-80%)
HP:0008064 Ichthyosis Very frequent (99-80%)
HP:0000962 Hyperkeratosis Frequent (79-30%)
HP:0000982 Palmoplantar keratoderma Frequent (79-30%)
HP:0001581 Recurrent skin infections Frequent (79-30%)
HP:0010783 Erythema Frequent (79-30%)
HP:0100326 Immunologic hypersensitivity Frequent (79-30%)
HP:0200034 Papule Frequent (79-30%)
HP:0000083 Renal insufficiency Occasional (29-5%)
HP:0002664 Neoplasm Occasional (29-5%)
HP:0002665 Lymphoma Occasional (29-5%)
HP:0002960 Autoimmunity Occasional (29-5%)
HP:0006775 Multiple myeloma Occasional (29-5%)
HP:0100242 Sarcoma Occasional (29-5%)


Phenotype(s) retrieved from case reports

    Total: 29

HPO ID Term # of case reports
HP:0010783 Erythema 4
HP:0001019 Erythroderma 3
HP:0000821 Hypothyroidism 2
HP:0000982 Palmoplantar keratoderma 2
HP:0005523 Lymphoproliferative disorder 2
HP:0030731 Carcinoma 2
HP:0100726 Kaposi's sarcoma 2
HP:0000956 Acanthosis nigricans 1
HP:0000962 Hyperkeratosis 1
HP:0000970 Anhidrosis 1
HP:0000989 Pruritus 1
HP:0000998 Hypertrichosis 1
HP:0001045 Vitiligo 1
HP:0001824 Weight loss 1
HP:0001880 Eosinophilia 1
HP:0002094 Dyspnea 1
HP:0002716 Lymphadenopathy 1
HP:0002860 Squamous cell carcinoma 1
HP:0004395 Malnutrition 1
HP:0008940 Generalized lymphadenopathy 1
HP:0011897 Neutrophilia 1
HP:0012219 Erythema nodosum 1
HP:0025142 Constitutional symptom 1
HP:0025508 Gottron's papules 1
HP:0030350 Erythematous papule 1
HP:0031287 Seborrheic keratosis 1
HP:0032061 Hypereosinophilia 1
HP:0100646 Thyroiditis 1
HP:0200036 Skin nodule 1


Causative gene(s) retrieved from Orphanet

    Total: 0

Gene Symbol Gene Name Entrez Gene ID