Porokeratosis [porokeratóza]

topical
11
Terms

diseminovaná superficiální aktinická porokeratóza
lineární porokeratóza
Mibelliho porokeratóza
palmární a plantární porokeratóza
porokeratosis disseminata superficialis et actinica
porokeratosis disseminata superficialis et actinica 2
porokeratosis linearis
porokeratosis Mibelli
porokeratosis palmaris et plantaris
porokeratosis punctata
potní žlázy - zrohovění vývodů

 

Disseminated Superficial Actinic Porokeratosis
Keratoderma Palmoplantar, Punctate Type 2
Porokeratosis of Mibelli
Porokeratosis Palmaris et Plantaris Disseminata
Porokeratosis Plantaris Palmaris et Disseminata
Porokeratosis Plantaris, Palmaris, Et Disseminata
Porokeratosis, Disseminated Superficial Actinic
Porokeratosis, Disseminated Superficial Actinic 2
Porokeratosis, Disseminated Superficial Actinic, 2
Porokeratosis, Linear
Porokeratosis, Mibelli
Porokeratosis, Palmar, Plantar, And Disseminated 1
Porokeratosis, Palmoplantar
Porokeratosis, Punctate
Type 2 Punctate PPK

Persistent link   https://www.medvik.cz/link/D017499
Definition

A heritable disorder of faulty keratinization characterized by the proliferation of abnormal clones of KERATINOCYTES and lesions showing varying atrophic patches surrounded by an elevated, keratotic border. These keratotic lesions can progress to overt cutaneous neoplasm. Several clinical variants are recognized, including porokeratosis of Mibelli, linear porokeratosis, disseminated superficial actinic porokeratosis, palmoplantar porokeratosis, and punctate porokeratosis.

Annotation
do not confuse with PARAKERATOSIS
DUI
D017499 MeSH Browser
CUI
M0026551
Previous indexing
Keratosis (1966-1992)
History note
93
Public note
93

Allowable subheadings

BL
blood
CF
cerebrospinal fluid
CI
chemically induced
CL
classification 2
CO
complications
DI
diagnosis 8
DG
diagnostic imaging
DH
diet therapy
DT
drug therapy 5
EC
economics
EM
embryology
EN
enzymology
EP
epidemiology
EH
ethnology
ET
etiology 3
GE
genetics
HI
history
IM
immunology
ME
metabolism
MI
microbiology
MO
mortality
NU
nursing
PS
parasitology
PA
pathology 1
PP
physiopathology
PC
prevention & control
PX
psychology
RT
radiotherapy
RH
rehabilitation
SU
surgery
TH
therapy 4
UR
urine
VE
veterinary
VI
virology

C Diseases
C16 Congenital, Hereditary, and Neonatal Diseases and Abnormalities 439
C16.320 Genetic Diseases, Inborn 1 215
C16.320.850 Skin Diseases, Genetic 89
C16.320.850.080 Albinism 17
C16.320.850.180 Cutis Laxa 10
C16.320.850.190 Darier Disease 26
C16.320.850.210 Dermatitis, Atopic 1 454
C16.320.850.235 Dyskeratosis Congenita 9
C16.320.850.250 Ectodermal Dysplasia 33
C16.320.850.260 Ehlers-Danlos Syndrome 51
C16.320.850.275 Epidermolysis Bullosa 108
C16.320.850.337 Erythrokeratodermia Variabilis 1
C16.320.850.368 Hyaline Fibromatosis Syndrome 1
C16.320.850.400 Ichthyosiform Erythroderma, Congenital 8
C16.320.850.402 Ichthyosis Bullosa of Siemens 3
C16.320.850.405 Ichthyosis Vulgaris 5
C16.320.850.408 Ichthyosis, X-Linked 9
C16.320.850.420 Incontinentia Pigmenti 19
C16.320.850.475 Keratoderma, Palmoplantar 15
C16.320.850.542 Leukokeratosis, Hereditary Mucosal 1
C16.320.850.595 Lipoid Proteinosis of Urbach and Wiethe 5
C16.320.850.647 Monilethrix 1
C16.320.850.673 Netherton Syndrome 2
C16.320.850.700 Pemphigus, Benign Familial 11
C16.320.850.730 Porokeratosis 11
C16.320.850.738 Porphyria, Erythropoietic 11
C16.320.850.742 Porphyrias, Hepatic 27
C16.320.850.746 Prolidase Deficiency
C16.320.850.750 Pseudoxanthoma Elasticum 13
C16.320.850.765 Rothmund-Thomson Syndrome 8
C16.320.850.820 Sjogren-Larsson Syndrome 4
C16.320.850.895 Trichothiodystrophy Syndromes 1
C16.320.850.970 Xeroderma Pigmentosum 25
C17 Skin and Connective Tissue Diseases 32
C17.800 Skin Diseases 2 801
C17.800.428 Keratosis 133
C17.800.428.200 Callosities 7
C17.800.428.260 Cholesteatoma 84
C17.800.428.275 Darier Disease 26
C17.800.428.304 Erythrokeratodermia Variabilis 1
C17.800.428.333 Ichthyosis 62
C17.800.428.435 Keratoderma, Palmoplantar 15
C17.800.428.570 Keratosis, Actinic 44
C17.800.428.580 Keratosis, Seborrheic 20
C17.800.428.736 Parakeratosis 10
C17.800.428.750 Porokeratosis 11
C17.800.827 Skin Diseases, Genetic 89
C17.800.827.080 Albinism 17
C17.800.827.180 Cutis Laxa 10
C17.800.827.190 Darier Disease 26
C17.800.827.210 Dermatitis, Atopic 1 454
C17.800.827.235 Dyskeratosis Congenita 9
C17.800.827.250 Ectodermal Dysplasia 33
C17.800.827.260 Ehlers-Danlos Syndrome 51
C17.800.827.275 Epidermolysis Bullosa 108
C17.800.827.337 Erythrokeratodermia Variabilis 1
C17.800.827.368 Hereditary Autoinflammatory Diseases 47
C17.800.827.384 Hyaline Fibromatosis Syndrome 1
C17.800.827.400 Ichthyosiform Erythroderma, Congenital 8
C17.800.827.403 Ichthyosis Bullosa of Siemens 3
C17.800.827.405 Ichthyosis Vulgaris 5
C17.800.827.408 Ichthyosis, X-Linked 9
C17.800.827.420 Incontinentia Pigmenti 19
C17.800.827.475 Keratoderma, Palmoplantar 15
C17.800.827.595 Leukokeratosis, Hereditary Mucosal 1
C17.800.827.602 Monilethrix 1
C17.800.827.610 Muir-Torre Syndrome 10
C17.800.827.655 Netherton Syndrome 2
C17.800.827.700 Pemphigus, Benign Familial 11
C17.800.827.730 Porokeratosis 11
C17.800.827.738 Porphyria, Erythropoietic 11
C17.800.827.742 Porphyrias, Hepatic 27
C17.800.827.750 Pseudoxanthoma Elasticum 13
C17.800.827.775 Rothmund-Thomson Syndrome 8
C17.800.827.820 Sjogren-Larsson Syndrome 4
C17.800.827.895 Trichothiodystrophy Syndromes 1
C17.800.827.970 Xeroderma Pigmentosum 25

Congenital facial linear porokeratosis Disease MeSH Browser

Craniosynostosis, anal anomalies, and porokeratosis Disease MeSH Browser

Porokeratosis punctata palmaris et plantaris Disease MeSH Browser

Porokeratosis, Disseminated Superficial Actinic, 3 Disease MeSH Browser

Porokeratosis, Disseminated Superficial Actinic, 4 Disease MeSH Browser

Porokeratosis, disseminated superficial actinic 1 Disease MeSH Browser

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