gms | German Medical Science

80. Jahresversammlung der Deutschen Gesellschaft für Hals-Nasen-Ohren-Heilkunde, Kopf- und Hals-Chirurgie e. V.

Deutsche Gesellschaft für Hals-Nasen-Ohren-Heilkunde, Kopf- und Hals-Chirurgie e. V.

20.05. - 24.05.2009, Rostock

Cutaneous large B-cell-lymphoma – a rare differential diagnosis of tumors of the outer nose

Meeting Abstract

  • corresponding author Karsten Koch - Department of ORL, SRH-Waldklinikum, Gera, Germany
  • Stephan Marciniak - Department of ORL, SRH-Waldklinikum, Gera, Germany
  • Gerhard Foerster - Department of ORL, SRH-Waldklinikum, Gera, Germany
  • Andreas Mueller - Department of ORL, SRH-Waldklinikum, Gera, Germany
  • Carsten Boltze - Institute of Pathology, SRH-Waldklinikum, Gera, Germany

German Society of Oto-Rhino-Laryngology, Head and Neck Surgery. 80th Annual Meeting of the German Society of Oto-Rhino-Laryngology, Head and Neck Surgery. Rostock, 20.-24.05.2009. Düsseldorf: German Medical Science GMS Publishing House; 2009. Doc09hno101

DOI: 10.3205/09hno101, URN: urn:nbn:de:0183-09hno1019

Veröffentlicht: 22. Juli 2009

© 2009 Koch et al.
Dieser Artikel ist ein Open Access-Artikel und steht unter den Creative Commons Lizenzbedingungen (http://creativecommons.org/licenses/by-nc-nd/3.0/deed.de). Er darf vervielfältigt, verbreitet und öffentlich zugänglich gemacht werden, vorausgesetzt dass Autor und Quelle genannt werden.


Gliederung

Text

Most malignant lesions of the outer nose are of epithelial origin. Basal cell carcinoma and spinocellular carcinoma are the most common entities. Benign or precancerous lesions are important differential diagnoses. Other tumor entities such as melanoma, sarcoma or lymphoma are comparatively rare.

Case: A 54-year-old male patient suffered from a destructive infiltrating tumor of the right nasal entrance. On first presentation we found a necrosis of the columella with an accompanying inflammation of the nasal and paranasal skin. Under the suspicion of a necrotizing inflammation affected parts of the anterior septum were removed combined with a local and systemic antibiotic treatment. Histopathology confirmed a necrotizing inflammation involving vessels comparable to a late stage of Wegner’s granulomatosis. However ANCA and ANA were negative. There was no evidence for abdominal, pulmonary or cerebral involvement.

Suspecting Wegner’s disease with false negative ANCA and local manifestation the patient was treated immunosuppressive with cyclophoshamid, later with azathioprine and prednisolon.

After a brief period of improvement disease progressed again resulting in an extensive septal perforation. A second histopathology specimen was taken and revealed a cutaneous large B-cell lymphoma. Treatment was changed to cyclophoshamide, doxorubicine, vincristine, rituximab as well as prednisolon.

Concurrent heavy inflammation can be misleading a correct diagnosis clinically as well as histopathologically. Only repeated biopsy after treatment of inflammation was able to find the real cause in our case. If there are discrepancies between clinical, histological and serological findings one should think of rare differential diagnosis too.