Hauttumorzentrum am Universitätsklinikum Freiburg Assigned diseases:
In the following you will find the diseases that are treated in this facility:
17q11 microdeletion syndrome
Acanthokeratolytic verrucous nevus
Adult T-cell leukemia/lymphoma
Aggressive primary cutaneous B-cell lymphoma
Aggressive primary cutaneous T-cell lymphoma
Angora hair nevus
Bannayan-Riley-Ruvalcaba syndrome
Bazex-Dupré-Christol syndrome
Becker nevus syndrome
Birt-Hogg-Dubé syndrome
Brooke-Spiegler syndrome
CHILD syndrome
CLAPO syndrome
CLOVES syndrome
Calcifying aponeurotic fibroma
Congenital panfollicular nevus
Congenital smooth muscle hamartoma
Cowden syndrome
Cutaneous neuroendocrine carcinoma
Cystic hygroma
Dermatofibrosarcoma protuberans
Didymosis aplasticosebacea
Diffuse lymphatic malformation
Epidermal nevus syndrome
Extranodal nasal NK/T cell lymphoma
Familial cylindromatosis
Familial hyperphosphatemic tumoral calcinosis/Hyperphosphatemic hyperostosis syndrome
Familial keratoacanthoma
Familial melanoma
Familial multiple fibrofolliculoma
Familial multiple trichoepithelioma
Familial normophosphatemic tumoral calcinosis
Familial tumoral calcinosis
Follicular atrophoderma-basal cell carcinoma
Gardner syndrome
Generalized basaloid follicular hamartoma syndrome
Gorlin syndrome
Granulomatous slack skin
Hemihyperplasia-multiple lipomatosis syndrome
Hereditary leiomyomatosis and renal cell cancer
Indolent primary cutaneous B-cell lymphoma
Indolent primary cutaneous T-cell lymphoma
Infantile digital fibromatosis
Infantile myofibromatosis
Inflammatory linear verrucous epidermal nevus
Large congenital melanocytic nevus
Ledderhose disease
Linear nevus sebaceus syndrome
Linear verrucous nevus syndrome
Macrocystic lymphatic malformation
Malignant melanoma of the mucosa
Microcystic lymphatic malformation
Muir-Torre syndrome
Multiple self-healing squamous epithelioma
Mycosis fungoides and variants
NEVADA syndrome
Neurocutaneous melanocytosis
Neurofibromatosis type 1
Neurofibromatosis type 1 due to NF1 mutation or intragenic deletion
Nevus comedonicus syndrome
Nevus of Ito
Nevus of Ota
Oley syndrome
Onychocytic matricoma
Onychomatricoma
PENS syndrome
PTEN hamartoma tumor syndrome
Phakomatosis pigmentokeratotica
Pilomatrixoma
Porokeratotic eccrine ostial and dermal duct nevus
Primary cutaneous B-cell lymphoma
Primary cutaneous CD30+ T-cell lymphoproliferative disease
Primary cutaneous CD4+ small/medium-sized pleomorphic T-cell lymphoma
Primary cutaneous T-cell lymphoma
Primary cutaneous aggressive epidermotropic CD8+ T-cell lymphoma
Primary cutaneous diffuse large B-cell lymphoma, leg type
Primary cutaneous follicle center lymphoma
Primary cutaneous gamma/delta-positive T-cell lymphoma
Primary cutaneous lymphoma
Primary cutaneous marginal zone B-cell lymphoma
Primary cutaneous peripheral T-cell lymphoma not otherwise specified
Proliferating trichilemmal cyst
Proteus syndrome
Proteus-like syndrome
Rare lymphatic malformation
Rare nail tumor
Rare nevus
Rare skin tumor or hamartoma
Rombo syndrome
SCALP syndrome
Segmental outgrowth-lipomatosis-arteriovenous malformation-epidermal nevus syndrome
Subcutaneous panniculitis-like T-cell lymphoma
Superficial fibromatosis
Syringocystadenoma papilliferum
Sézary syndrome
Trichofolliculoma
Verrucous nevus
White sponge nevus