[Clinical pathological aspects of Mazabraud's syndrome]

Standard

[Clinical pathological aspects of Mazabraud's syndrome]. / Pollandt, K; Lohmann, Christoph; Werner, M; Delling, G.

In: PATHOLOGE, Vol. 23, No. 5, 5, 2002, p. 357-360.

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

Harvard

Pollandt, K, Lohmann, C, Werner, M & Delling, G 2002, '[Clinical pathological aspects of Mazabraud's syndrome]', PATHOLOGE, vol. 23, no. 5, 5, pp. 357-360. <http://www.ncbi.nlm.nih.gov/pubmed/12376861?dopt=Citation>

APA

Pollandt, K., Lohmann, C., Werner, M., & Delling, G. (2002). [Clinical pathological aspects of Mazabraud's syndrome]. PATHOLOGE, 23(5), 357-360. [5]. http://www.ncbi.nlm.nih.gov/pubmed/12376861?dopt=Citation

Vancouver

Pollandt K, Lohmann C, Werner M, Delling G. [Clinical pathological aspects of Mazabraud's syndrome]. PATHOLOGE. 2002;23(5):357-360. 5.

Bibtex

@article{5dda08d1ff7b42ef8b168b3d7fa646ae,
title = "[Clinical pathological aspects of Mazabraud's syndrome]",
abstract = "Mazabraud's syndrome is a rare, sporadic disorder characterised by the association of mainly polyostotic fibrous dysplasia and intramuscular myxoma. Fibrous dysplasia is mostly diagnosed at a younger age, while myxomas only occur during adulthood. We report a case of a 42-year-old female with Mazabraud's syndrome where a polyostotic fibrous dysplasia was already diagnosed and at presentation two newly formed intramuscular myxomas were found in the gluteal muscle.",
author = "K Pollandt and Christoph Lohmann and M Werner and G Delling",
year = "2002",
language = "Deutsch",
volume = "23",
pages = "357--360",
journal = "PATHOLOGE",
issn = "0172-8113",
publisher = "Springer",
number = "5",

}

RIS

TY - JOUR

T1 - [Clinical pathological aspects of Mazabraud's syndrome]

AU - Pollandt, K

AU - Lohmann, Christoph

AU - Werner, M

AU - Delling, G

PY - 2002

Y1 - 2002

N2 - Mazabraud's syndrome is a rare, sporadic disorder characterised by the association of mainly polyostotic fibrous dysplasia and intramuscular myxoma. Fibrous dysplasia is mostly diagnosed at a younger age, while myxomas only occur during adulthood. We report a case of a 42-year-old female with Mazabraud's syndrome where a polyostotic fibrous dysplasia was already diagnosed and at presentation two newly formed intramuscular myxomas were found in the gluteal muscle.

AB - Mazabraud's syndrome is a rare, sporadic disorder characterised by the association of mainly polyostotic fibrous dysplasia and intramuscular myxoma. Fibrous dysplasia is mostly diagnosed at a younger age, while myxomas only occur during adulthood. We report a case of a 42-year-old female with Mazabraud's syndrome where a polyostotic fibrous dysplasia was already diagnosed and at presentation two newly formed intramuscular myxomas were found in the gluteal muscle.

M3 - SCORING: Zeitschriftenaufsatz

VL - 23

SP - 357

EP - 360

JO - PATHOLOGE

JF - PATHOLOGE

SN - 0172-8113

IS - 5

M1 - 5

ER -