Histiocytoid cardiomyopathy

Histiocytoid cardiomyopathy is an arrhythmogenic disorder characterised by cardiomegaly, severe cardiac arrhythmias or sudden death, and the presence of histiocyte-like cells within the myocardium.



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Narrow down the case reports



Total: 31 (papers)

  


(per page)
Matched Phenotype  Gene  Mutation  MeSH
Rank
(Similarity)
PMID
(PMCID)
7
(4.0%)
8563940
Histiocytoid cardiomyopathy with hypotonia in an infant.
Otani M, Hoshida H, Saji T, Matsuo N, Kawamura S.
Pathol Int. 1995;45(10):774-80.
Cardiac arrest
Cardiac Arrest Cardiomyopathies Electrocardiography Electron Microscopy Fatal Outcome Females Histiocytosis Homo sapiens Infant Mitochondria Myofibrils Tachycardia, Ventricular
7
(4.0%)
8263485
Histiocytoid cardiomyopathy: case report and literature review.
Prahlow JA, Teot LA.
J Forensic Sci. 1993;38(6):1427-35.
Ventricular fibrillation
Cardiac Arrest Cardiomyopathies Electron Microscopy Fatal Outcome Females Homo sapiens Infant
7
(4.0%)
8244322
Infantile histiocytoid cardiomyopathy--myocardial or conduction system hamartoma: what is the cell type involved?
Gelb AB, Van Meter SH, Billingham ME, Berry GJ, Rouse RV.
Hum Pathol. 1993;24(11):1226-31.
Sudden cardiac death
CD68
Actins Autopsy Cardiomyopathies Differential Diagnosis Electron Microscopy Females Heart Neoplasm Hemangioma Histiocytes Homo sapiens Immunohistochemistry Infant Infant, Newborn Myocardium
7
(4.0%)
7942464
Infantile histiocytoid cardiomyopathy: three cases and literature review.
Malhotra V, Ferrans VJ, Virmani R.
Am Heart J. 1994;128(5):1009-21.
Cardiomyopathy
Cardiomyopathies Child, Preschool Congenital Heart Defects Females Histiocytes Homo sapiens Infant Infant, Newborn Male Myocardium
7
(4.0%)
7771390
Sudden death in an infant due to histiocytoid cardiomyopathy. A light-microscopic, ultrastructural, and immunohistochemical study.
Ruszkiewicz AR, Vernon-Roberts E.
Am J Forensic Med Pathol. 1995;16(1):74-80.
Arrhythmia
Cardiomyopathies Histiocytosis Homo sapiens Immunohistochemistry Infant Male Sudden Cardiac Death
7
(4.0%)
6778813
Oncocytic cardiomyopathy in an infant with oncocytosis in exocrine and endocrine glands.
Silver MM, Burns JE, Sethi RK, Rowe RD.
Hum Pathol. 1980;11(6):598-605.
Cardiomyopathy
DCAF7
Cardiomyopathies Eye Abnormalities Females Homo sapiens Infant Myocardium Neoplastic Cell Transformation Pituitary Gland, Anterior Salivary Glands Sublingual Gland Thyroid Gland
7
(4.0%)
6093033
Histiocytoid cardiomyopathy of infancy: deficiency of reducible cytochrome b in heart mitochondria.
Papadimitriou A, Neustein HB, Dimauro S, Stanton R, Bresolin N.
Pediatr Res. 1984;18(10):1023-8.
Cardiomegaly
CCL14 CYCS MT-CYB
Cardiomyopathies Cytochrome b Group Cytochrome-c Oxidase Deficiency Electrocardiography Females Histiocytes Homo sapiens Infant, Newborn Mitochondria, Heart Myocardium Oxidation-Reduction Succinate Cytochrome c Oxidoreductase
7
(4.0%)
4083007
A case of foamy myocardial transformation of infancy.
Yutani C, Imakita M, Ishibashi-Ueda H, Kamiya T, Aragaki Y.
Acta Pathol Jpn. 1985;35(5):1255-65.
Cardiomyopathy
Cardiomyopathies Electrocardiography Electron Microscopy Females Homo sapiens Infant Sex Factors Tachycardia
7
(4.0%)
3558867
Foamy myocardial transformation of infancy: an inherited disease.
Suarez V, Fuggle WJ, Cameron AH, French TA, Hollingworth T.
J Clin Pathol. 1987;40(3):329-34.
Arrhythmia
Cardiomyopathies Females Homo sapiens Infant Male Mitochondria, Heart
7
(4.0%)
3310564
Oncocytic cardiomyopathy of infancy with Wolff-Parkinson-White syndrome and ectopic foci causing tachydysrhythmias in children.
Keller BB, Mehta AV, Shamszadeh M, Marino TA, Sanchez GR, Huff DS, Dunn JM.
Am Heart J. 1987;114(4 Pt 1):782-92.
Cardiomyopathy
Cardiomyopathies Echocardiography Electrocardiography Females Homo sapiens Infant Myocardium Wolff-Parkinson-White Syndrome
        

Phenotype(s) retrieved from Orphanet

    Total: 0

HPO ID Term Frequency


Phenotype(s) retrieved from case reports

    Total: 11

HPO ID Term # of case reports
HP:0011675 Arrhythmia 4
HP:0000568 Microphthalmia 3
HP:0010566 Hamartoma 3
HP:0001638 Cardiomyopathy 2
HP:0001716 Wolff-Parkinson-White syndrome 2
HP:0009729 Cardiac rhabdomyoma 2
HP:0001645 Sudden cardiac death 1
HP:0001695 Cardiac arrest 1
HP:0003128 Lactic acidosis 1
HP:0009730 Rhabdomyoma 1
HP:0010617 Cardiac fibroma 1


Causative gene(s) retrieved from Orphanet

    Total: 1

Gene Symbol Gene Name Entrez Gene ID
MT-CYB mitochondrially encoded cytochrome b 4519