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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Total: 31 (papers)

  


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Matched Phenotype  Gene  Mutation  MeSH
Rank
(Similarity)
PMID
(PMCID)
7
(4.0%)
24099092
Orthotopic heart transplantation in two infants with histiocytoid cardiomyopathy and left ventricular non-compaction.
Siehr SL, Bernstein D, Yeh J, Berry GJ, Rosenthal DN, Hollander SA.
Pediatr Transplant. 2013;17(7):E165-7.
Congestive heart failure
Cardiomyopathies Cardiomyopathy, Dilated Electron Transport Complex III Extracorporeal Membrane Oxygenation Females Heart Heart Transplantation Heart Ventricle Heart-Assist Devices Homo sapiens Infant Male Shock, Cardiogenic
7
(4.0%)
22839721
[Histiocytoid cardiomyopathy in an infant].
Bregel' LV, Belozerov IuM, Ogloblina ML, Golubev SS, Zemchenko OA, Pavlenok KN, Antoshkina EP, Bochkareva AK, Popod'ko TN.
Kardiologiia. 2012;52(7):93-6.
Cardiomegaly
Anti-Arrhythmia Agents Cardiomegaly Cardiomyopathies Cytochromes b Electron Transport Complex III Fatal Outcome Females Foam Cells Histocytochemistry Homo sapiens Infant Mitochondria, Heart Mutation Ventricular Flutter
7
(4.0%)
21601113
[A rare cause of sudden cardiac failure: histiocytoid cardiomyopathy].
Coulibaly B, Piercecchi-Marti MD, Fernandez C, Wasier AP, Viard L, Fraisse A, Figarella-Branger D, Leonetti G, Camboulives J, Paut O.
Ann Pathol. 2011;31(2):93-7.
Cardiomyopathy
Cardiomyopathies Electron Transport Complex III Fatal Outcome Females Homo sapiens Infant Sudden Cardiac Death
7
(4.0%)
16393567
[Histiocytoid cardiomyopathy. A rare cause of ventricular tachycardia and sudden cardiac death in small children].
Aksglaede L, Graem N, Jacobsen JR.
Ugeskr Laeger. 2006;168(1):61-2.
Sudden cardiac death
Cardiomyopathies Fatal Outcome Females Histiocytes Homo sapiens Infant Sudden Cardiac Death Tachycardia, Ventricular
7
(4.0%)
15157052
Demonstration of MyoD1 expression in oncocytic cardiomyopathy: report of two cases and review of the literature.
Hotarkova S, Hermanova M, Povysilova V, Dvorak K, Feit J, Lukas Z, Kren L, Vit P, Jicinska H, Hucin B.
Pathol Res Pract. 2004;200(1):59-65.
Arrhythmia
MYOD1
Cardiomyopathies Child Congenital Heart Defects Electron Microscopy Females Homo sapiens Immunohistochemistry Infant Infant, Newborn MyoD Protein Myocardium Oxyphil Cells
7
(4.0%)
12900578
Microphthalmia with linear skin defects syndrome (MLS): a male with a mosaic paracentric inversion of Xp.
Kutsche K, Werner W, Bartsch O, von der Wense A, Meinecke P, Gal A.
Cytogenet Genome Res. 2002;99(1-4):297-302.
Microphthalmia
ARHGAP6
Chromosomes, Human, X Fatal Outcome Fluorescent in Situ Hybridization GTPase-Activating Proteins Homo sapiens Infant Male Microphthalmos Mosaicism Sex Chromosome Aberrations Skin Abnormalities Syndrome
7
(4.0%)
10695541
Sudden cardiac death in infancy due to histiocytoid cardiomyopathy.
Grech V, Ellul B, Montalto SA.
Cardiol Young. 2000;10(1):49-51.
Sudden cardiac death
Autopsy Differential Diagnosis Females Histiocytosis Homo sapiens Hypertrophic Cardiomyopathy Infant Sudden Cardiac Death
7
(4.0%)
10463272
Histiocytoid cardiomyopathy: three new cases and a review of the literature.
Shehata BM, Patterson K, Thomas JE, Scala-Barnett D, Dasu S, Robinson HB.
Pediatr Dev Pathol. 1998;1(1):56-69.
Arrhythmia
Autopsy Cardiac Arrhythmia Cardiomyopathies Child, Preschool Chromosome Aberrations Fatal Outcome Females Histiocytes Homo sapiens Infant Infant, Newborn Male Mitochondria, Heart Myocardium Myofibrils X Chromosome
7
(4.0%)
9029929
Oncocytic cardiomyopathy: a rare cause of unexpected early childhood death associated with fitting.
Stahl J, Couper RT, Byard RW.
Med Sci Law. 1997;37(1):84-7.
Vomiting
Autopsy Cardiac Arrhythmia Cardiomyopathies Fatal Outcome Females Homo sapiens Infant Myocardium Seizures
7
(4.0%)
8617487
Histiocytoid cardiomyopathy and sudden death.
Koponen MA, Siegel RJ.
Hum Pathol. 1996;27(4):420-3.
Arrhythmia
Cardiomyopathies Fatal Outcome Females Homo sapiens Infant Sudden Cardiac Death
        

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