@techreport{KneitzBroeckerBecker2010,
  author    = {Kneitz, H. and Br{\"o}cker, Eva B. and Becker, JC},
  title     = {Mycosis fungoides bullosa: a case report and review of the literature},
  url       = {http://nbn-resolving.de/urn:nbn:de:bvb:20-opus-68233},
  year      = {2010},
  abstract  = {Introduction: Mycosis fungoides, the most common type of cutaneous T-cell lymphoma, can manifest in a variety of clinical and histological forms. Bulla formation is an uncommon finding in mycosis fungoides and only approximately 20 cases have been reported in the literature. Case presentation: We present a case of rapidly progressive mycosis fungoides in a 68-year-old Caucasian man who initially presented with erythematous plaques characterised by blister formation. Conclusion: Although mycosis fungoides bullosa is extremely rare, it has to be regarded as an important clinical subtype of cutaneous T-cell lymphoma. Mycosis fungoides bullosa represents a particularly aggressive form of mycosis fungoides and is associated with a poor prognosis. The rapid disease progression in our patient confirms bulla formation as an adverse prognostic sign in cutaneous T-cell lymphoma.},
  subject      = {Mycosis fungoides bullosa},
  language  = {en}
}