Epidermolysis bullosa (EB)

Types

Sunburn , Pemphigus , Albinism , Vitiligo , Viral Hepatitis , General , EB Simplex , Junctional , Dystrophic (Recessive-RDEB or Dominant- DDEB) , Epidermolysis bullosa acquisita , Bullous pemphigoid , Mucus membrane pemphigoid , Ocular cicatricial pemphigoid , Pemphigus vulgaris , Pemphigus foliaceus , General , Acute dermatitis (eczema) , Chronic dermatitis , Subacute dermatitis , Atopic Dermatitis (AD) , Stasis Dermatitis (SD) , Lichen Simplex Chronicus (LSC) , Contact Dermatitis - Irritant , Contact Dermatitis - Allergic (ACD) , Seborrheic Dermatitis , Bacterial folliculitis , Hot tub folliculitis , Verruca vulgaris , Verruca plantaris , Condylomata acuminata , Filiform warts , Verruca plana , Sclerosteosis , Van Buchem , Worth type , Acute , Chronic , Hematogenous , Contiguous , Acute bacterial , Chronic septic arthritis , Disseminated gonococcial infection (DGI) , Early (<3m after surgery) , Delayed (3-24m) , Late (>2y) , Classical , Hypermobility , Arthrochalasia , Vascular , Dermatosparaxis , Kyphoscoliosis , Duchenne MD , Becker's MD , Myotonic dystrophy type I , Acute , Chronic , Monomicrobial , Polymicrobial , Giant Melanocytic Nevus , Polyostotic Monostotic , Autosomal recessive infantile malignant (ARO) , Autosomal dominant (Albers-Schonberg) (ARO) , Camurati-Engelmann , Benign , Benign , Benign , McArdle's disease , Carnitine palmitoyltransferase II deficiency , Mitochondrial myopathy , Dermatomyositis , Polymyositis , Inclusion body myopathy , Soft tissue pain disorder , Episodic monoarticular Polyarticular Tophaceous gout , Central core disease , Basal Cell Nevus Syndrome (BCNS) , Xeroderma pigmentosum (XP) , Sun tan , Ichthyosis , Psoriasis , Ectodermal Dysplasia , Keloid , Acne , Tinea versicolor , Molluscum Contagiosum , Varicella Zoster Virus (VZV) (Shingles) , Scabies , Eryisipelas , Gas gangrene (myonecrosis) , Osteoporosis , Pycnodysostosis , Carbonic Anhydrase II deficiency , Fibrodysplasia ossificans progressive (FOP) , Marfan Syndrome , Stickler Syndrome , Achondroplasia , Polymyalgia Rheumatica (PR)

Disease Overview

Assuming it makes medical sense to have all the whole disease described here, we'll have a general description here.

Defining Characteristics

Verruca vulgaris
Verrucus (bumpy/rough), hyperkeratotic skin colored papules; usually asymptomatic unless 2ndary infection/inflammation

Verruca plantaris
Hyperkeratotic papules/plaques that are less exophytic, black macules of thrombosed capillary loops (“seeds” = lay term)

Condylomata acuminata Genital warts; flatter, gray/brown papules

Filiform warts
Thinlike projections common on face

Verruca plana
Pinkish warts common on hands/face

Disease Development

Verruca vulgaris
“Infection of basal layer of skin with HPV (dsDNA virus), resulting in the slow division of cells in the spinous layer; eventually leads to hyperkeratosis and papillomatosis
Transmitted from skin to skin contact, autoinoculation, contaminated surfaces”

Verruca plantaris
“Infection of basal layer of skin with HPV (dsDNA virus), resulting in the slow division of cells in the spinous layer; eventually leads to hyperkeratosis and papillomatosis
Transmitted from skin to skin contact, autoinoculation, contaminated surfaces”

Condylomata acuminata
“Infection of basal layer of skin with HPV (dsDNA virus), resulting in the slow division of cells in the spinous layer; eventually leads to hyperkeratosis and papillomatosis
Transmitted from skin to skin contact, autoinoculation, contaminated surfaces”