Almut Böer-Auer

Prof. Dr. Almut Böer-Auer

orcid

Research Focus & Metrics

Academic Career Length

23Years (2004-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

View All Publications
1 July 2007 in British Journal of Dermatology
Verified
Journal Article
Closed access
PDF file
JRJ. Röglin
J. Röglin
ABAlmut Böer-Auer
Almut Böer-Auer

17 July 2008 in British Journal of Dermatology
Verified
Journal Article
Closed access
PDF file
ABAlmut Böer-Auer
Almut Böer-Auer
RTR. Tirumalae
R. Tirumalae
MBM. Bresch
M. Bresch
TFT.M. Falk
T.M. Falk

6 June 2006 in British Journal of Dermatology
Verified
Journal Article
Closed access
PDF file
ABAlmut Böer-Auer
Almut Böer-Auer
NBN. Blödorn-Schlicht
N. Blödorn-Schlicht
DWD. Wiebels
D. Wiebels
VSV. Steinkraus
V. Steinkraus
TFT.M. Falk
T.M. Falk

24 January 2006 in British Journal of Dermatology
Verified
Journal Article
Closed access
PDF file
ABAlmut Böer-Auer
Almut Böer-Auer
NHN. Herder
N. Herder
KWK. Winter
K. Winter
TFT. Falk
T. Falk

1 June 2006 in The American Journal of Dermatopathology
Verified
Journal Article
Closed access
ABAlmut Böer-Auer
Almut Böer-Auer
It has been a subject of controversy whether keratosis lichenoides chronica (KLC) is a distinctive inflammatory disease of the skin or whether it represents a manifestation of another well-known disease, such as lichen planus, lupus erythematosus, or lichen simplex chronicus. In search of clear criteria for diagnosis of KLC the entire literature pertinent to the subject was studied and findings clinical and histopathologic as they were telegraphed in them were compared with a patient of my own experience. Review of the literature reveals more than 60 patients in whom the diagnosis of KLC was made. Three categories emerge based on whether the findings presented in a particular article (1) do not permit any diagnosis to be rendered; (2) do allow a diagnosis specific to be made, such as of lichen simplex, lichen planus, or lupus erythematosus; or (3) do not correspond to any disease well defined, such as lichen simplex, lichen planus, lupus erythematosus, but seem to show attributes morphologic, clinically and histopathologically, that are repeatable. Patients diagnosed as having KLC obviously represent a potpourri of different diseases, the most common of them being lichen simplex chronicus, lichen planus, and lupus erythematosus. Fewer than 25 patients reported on, however, presented themselves with lesions very similar to one another clinically, namely, an eruption that involved the face in a manner reminiscent of seborrheic dermatitis and with tiny papules on the trunk and extremities, which assumed linear and reticulate shapes by way of confluence of lesions. Individual papules were infundibulocentric and acrosyringocentric. Findings histopathologic were those of a lichenoid interface dermatitis affiliated with numerous necrotic keratocytes and covered by parakeratosis housing neutrophils in staggered fashion. These patients seem to have an authentic and distinctive condition that is exceedingly rare. In conclusion, the diagnosis of KLC should be made only for patients who present themselves with features clinical and findings histopathologic that resemble closely those of what is summarized in this article under category 3.

1 May 2006 in Journal of the American Academy of Dermatology
Verified
Journal Article
Closed access
ABAlmut Böer-Auer
Almut Böer-Auer
TFThomas M. Falk
Thomas M. Falk