Der interessante Fall Nr. 63

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Der interessante Fall Nr. 63. / Münscher, A; Lessle, M; Grundmann, T.

In: LARYNGO RHINO OTOL, Vol. 83, No. 9, 09.2004, p. 617-9.

Research output: SCORING: Contribution to journalSCORING: Journal articleResearchpeer-review

Harvard

Münscher, A, Lessle, M & Grundmann, T 2004, 'Der interessante Fall Nr. 63', LARYNGO RHINO OTOL, vol. 83, no. 9, pp. 617-9. https://doi.org/10.1055/s-2004-825748

APA

Münscher, A., Lessle, M., & Grundmann, T. (2004). Der interessante Fall Nr. 63. LARYNGO RHINO OTOL, 83(9), 617-9. https://doi.org/10.1055/s-2004-825748

Vancouver

Münscher A, Lessle M, Grundmann T. Der interessante Fall Nr. 63. LARYNGO RHINO OTOL. 2004 Sep;83(9):617-9. https://doi.org/10.1055/s-2004-825748

Bibtex

@article{afbf9ef76b984443a6c9874bbb5450eb,
title = "Der interessante Fall Nr. 63",
abstract = "Angiosarcomas are rare, aggressive tumors of vascular origin. They occur most often in areas of long term sun exposed skin in the elderly, in long standing lymphoedema or after radiation therapy. The prognosis is poor, radical surgery required, in addition radiation or chemo-therapy are considered to be therapeutical options. We report on a male patient, 70 years old with a slightly bleeding blueish tumor encompassing the complete nose. This patient treated with several antibiotics while continuous growth led to the described course. After 4 months a biopsy was taken revealing an angiosarcoma of the nose. Subsequently the patient was referred to our department and due to staging results a surgical therapy (ablatio nasi) followed. The final histological diagnosis was a low grade angiosarcoma of the cutaneous and subcutaneous tissue of the nose without infiltration of bone or cartilage, confirmed by immunohistological staining. Angiosarcomas of the head and neck region are extremely rare. Especially only few cases of nasal angiosarcoma infiltrating the complete nose are described in literature. Prognosis, therapy and differential diagnosis have to be discussed.",
keywords = "Aged, Biopsy, Hemangiosarcoma, Humans, Male, Nose, Nose Neoplasms, Prognosis, Skin, Skin Neoplasms, Surgical Flaps",
author = "A M{\"u}nscher and M Lessle and T Grundmann",
year = "2004",
month = sep,
doi = "10.1055/s-2004-825748",
language = "Deutsch",
volume = "83",
pages = "617--9",
journal = "LARYNGO RHINO OTOL",
issn = "0935-8943",
publisher = "Georg Thieme Verlag KG",
number = "9",

}

RIS

TY - JOUR

T1 - Der interessante Fall Nr. 63

AU - Münscher, A

AU - Lessle, M

AU - Grundmann, T

PY - 2004/9

Y1 - 2004/9

N2 - Angiosarcomas are rare, aggressive tumors of vascular origin. They occur most often in areas of long term sun exposed skin in the elderly, in long standing lymphoedema or after radiation therapy. The prognosis is poor, radical surgery required, in addition radiation or chemo-therapy are considered to be therapeutical options. We report on a male patient, 70 years old with a slightly bleeding blueish tumor encompassing the complete nose. This patient treated with several antibiotics while continuous growth led to the described course. After 4 months a biopsy was taken revealing an angiosarcoma of the nose. Subsequently the patient was referred to our department and due to staging results a surgical therapy (ablatio nasi) followed. The final histological diagnosis was a low grade angiosarcoma of the cutaneous and subcutaneous tissue of the nose without infiltration of bone or cartilage, confirmed by immunohistological staining. Angiosarcomas of the head and neck region are extremely rare. Especially only few cases of nasal angiosarcoma infiltrating the complete nose are described in literature. Prognosis, therapy and differential diagnosis have to be discussed.

AB - Angiosarcomas are rare, aggressive tumors of vascular origin. They occur most often in areas of long term sun exposed skin in the elderly, in long standing lymphoedema or after radiation therapy. The prognosis is poor, radical surgery required, in addition radiation or chemo-therapy are considered to be therapeutical options. We report on a male patient, 70 years old with a slightly bleeding blueish tumor encompassing the complete nose. This patient treated with several antibiotics while continuous growth led to the described course. After 4 months a biopsy was taken revealing an angiosarcoma of the nose. Subsequently the patient was referred to our department and due to staging results a surgical therapy (ablatio nasi) followed. The final histological diagnosis was a low grade angiosarcoma of the cutaneous and subcutaneous tissue of the nose without infiltration of bone or cartilage, confirmed by immunohistological staining. Angiosarcomas of the head and neck region are extremely rare. Especially only few cases of nasal angiosarcoma infiltrating the complete nose are described in literature. Prognosis, therapy and differential diagnosis have to be discussed.

KW - Aged

KW - Biopsy

KW - Hemangiosarcoma

KW - Humans

KW - Male

KW - Nose

KW - Nose Neoplasms

KW - Prognosis

KW - Skin

KW - Skin Neoplasms

KW - Surgical Flaps

U2 - 10.1055/s-2004-825748

DO - 10.1055/s-2004-825748

M3 - SCORING: Zeitschriftenaufsatz

C2 - 15372345

VL - 83

SP - 617

EP - 619

JO - LARYNGO RHINO OTOL

JF - LARYNGO RHINO OTOL

SN - 0935-8943

IS - 9

ER -