Hauttumorzentrum am Universitätsklinikum Freiburg
Description of facility
Director / Spokesperson
PD Dr. Frank MeißInformation
Care facility for adults and childrenDescription
Das Hauttumorzentrum Freiburg ist unter dem Dach des Tumorzentrum Freiburg - CCCF gegründet worden und ist ein Kompetenzzentrum zur Versorgung von Patienten mit bösartigen Neubildungen der Haut. Die interdisziplinäre Vernetzung mit den Kooperationspartnern am Universitätsklinikum Freiburg sowie mit den niedergelassenen Behandlungspartnern der Region ermöglichen eine optimale Patientenversorgung. Diese beinhaltet u.a. die interdisziplinäre Tumorkonferenz bei der fachübergreifende Fragen hinsichtlich Diagnostik und Therapie besprochen und abgestimmt werden. Darüber hinaus bietet das Hauttumorzentrum neben den leitliniengerechten Therapieoptionen für Hauttumorpatienten die Teilnahme an Therapiestudien, die Zugang zu Therapieoptionen nach den neusten wissenschaftlichen Erkenntnissen gewährleisten.
Consultation hours
nach Vereinbarung.
Care provisions
This facility offers the following
- Diagnostic
- Therapy
Contact
Sekretariat
0761 27067951
0761 27067950
dermato-onkologie@uniklinik-freiburg.de
Website
https://www.uniklinik-freiburg.de/hautklinik/hauttumorzentrum.html
Languages
Deutsch Englisch
Preview of the assigned diseases 4
Mycosis fungoides and variants
Primary cutaneous B-cell lymphoma
17q11 microdeletion syndrome
Onychocytic matricoma
PTEN hamartoma tumor syndrome
Pilomatrixoma
NEVADA syndrome
Cutaneous neuroendocrine carcinoma
Onychomatricoma
Muir-Torre syndrome
Familial normophosphatemic tumoral calcinosis
Trichofolliculoma
Diffuse lymphatic malformation
Familial multiple trichoepithelioma
Rare nail tumor
Primary cutaneous T-cell lymphoma
CLOVES syndrome
Generalized basaloid follicular hamartoma syndrome
Nevus of Ota
Familial hyperphosphatemic tumoral calcinosis/Hyperphosphatemic hyperostosis syndrome
Congenital smooth muscle hamartoma
Proteus syndrome
Cowden syndrome
Nevus of Ito
Familial multiple fibrofolliculoma
Familial melanoma
Epidermal nevus syndrome
Familial cylindromatosis
Follicular atrophoderma-basal cell carcinoma
Oley syndrome
Large congenital melanocytic nevus
Proliferating trichilemmal cyst
Neurofibromatosis type 1 due to NF1 mutation or intragenic deletion
Familial keratoacanthoma
Verrucous nevus
Inflammatory linear verrucous epidermal nevus
Acanthokeratolytic verrucous nevus
Neurofibromatosis type 1
Hemihyperplasia-multiple lipomatosis syndrome
PENS syndrome
Rare lymphatic malformation
Nevus comedonicus syndrome
Gorlin syndrome
Granulomatous slack skin
Proteus-like syndrome
Cystic hygroma
Becker nevus syndrome
Bannayan-Riley-Ruvalcaba syndrome
Rombo syndrome
Macrocystic lymphatic malformation
Microcystic lymphatic malformation
Brooke-Spiegler syndrome
Familial tumoral calcinosis
Bazex-Dupré-Christol syndrome
Hereditary leiomyomatosis and renal cell cancer
Ledderhose disease
Primary cutaneous CD4+ small/medium-sized pleomorphic T-cell lymphoma
Birt-Hogg-Dubé syndrome
Primary cutaneous aggressive epidermotropic CD8+ T-cell lymphoma
Superficial fibromatosis
Segmental outgrowth-lipomatosis-arteriovenous malformation-epidermal nevus syndrome
CLAPO syndrome
Adult T-cell leukemia/lymphoma
Rare nevus
Primary cutaneous CD30+ T-cell lymphoproliferative disease
Calcifying aponeurotic fibroma
Primary cutaneous lymphoma
Extranodal nasal NK/T cell lymphoma
Infantile digital fibromatosis
Primary cutaneous marginal zone B-cell lymphoma
Primary cutaneous gamma/delta-positive T-cell lymphoma
Infantile myofibromatosis
CHILD syndrome
Primary cutaneous follicle center lymphoma
Subcutaneous panniculitis-like T-cell lymphoma
Primary cutaneous peripheral T-cell lymphoma not otherwise specified
Rare skin tumor or hamartoma
Primary cutaneous diffuse large B-cell lymphoma, leg type
Multiple self-healing squamous epithelioma
White sponge nevus
Indolent primary cutaneous T-cell lymphoma
Phakomatosis pigmentokeratotica
Gardner syndrome
Malignant melanoma of the mucosa
Didymosis aplasticosebacea
Angora hair nevus
Dermatofibrosarcoma protuberans
Aggressive primary cutaneous T-cell lymphoma
Linear verrucous nevus syndrome
Indolent primary cutaneous B-cell lymphoma
SCALP syndrome
Aggressive primary cutaneous B-cell lymphoma
Linear nevus sebaceus syndrome
Syringocystadenoma papilliferum
Porokeratotic eccrine ostial and dermal duct nevus
Congenital panfollicular nevus
Sézary syndrome
Neurocutaneous melanocytosis
7.85909771919250648.00786953281264Hauttumorzentrum am Universitätsklinikum Freiburg
Last updated:
17.07.2023