Registry

The development of the registry of very rare hematooncologic diagnoses was supported by an internal grant of the University Hospital Brno. In this pilot and also unique project, patients followed-up at our department have been enrolled.

Enter the registry


Numbers of recorded patients as on 18.1.2019 [N = 129]

 

Overview of individual diagnoses in recorded patients

DiagnosisType
Castleman diseaseMulticentric Castleman disease
Castleman diseaseUnicentric Castleman disease
Cutaneous manifestations of monoclonal gammopathiesCold agglutinin disease
Cutaneous manifestations of monoclonal gammopathiesCryoglobulinemia
Cutaneous manifestations of monoclonal gammopathiesDiffuse plane normolipemic xanthomatosis
Cutaneous manifestations of monoclonal gammopathiesNecrobiotic xanthogranuloma
Cutaneous manifestations of monoclonal gammopathiesSchnitzler syndrome
Cutaneous manifestations of monoclonal gammopathiesScleredema
Cutaneous manifestations of monoclonal gammopathiesScleromyxedema
Cutaneous manifestations of monoclonal gammopathiesSubcorneal pustular dermatosis type of IgA pemphigus
HistiocytosesAdult-onset periocular xanthogranuloma
HistiocytosesErdheim-Chester disease
HistiocytosesFollicular dendritic cell sarcoma
HistiocytosesHistiocytic sarcoma
HistiocytosesInterdigitating dendritic cell sarcoma
HistiocytosesKikuchi-Fujimoto disease
HistiocytosesLangerhans cell histiocytosis
HistiocytosesRosai-Dorfman disease
MastocytosesAggressive SM
MastocytosesIndolent SM (isolated bone marrow mastocytosis)
VasculopathyAggressive solitary angioma
VasculopathyAngiosarcoma
VasculopathyHereditary hemorrhagic telangiectasia
VasculopathyMultiple angiomatosis