Successful treatment of pustulosis palmaris et plantaris with granulocyte colony stimulating factor in a patient with hereditary neutropenia. View Full Text


Ontology type: schema:ScholarlyArticle      Open Access: True


Article Info

DATE

1998

AUTHORS

M Hino, T Yamane, T Kuwaki, T Kono, S Kitagawa, N Tatsumi

ABSTRACT

A 26-year-old female with hereditary neutropenia had Pustulosis Palmaris et Plantaris. Drug administration did not improve her symptoms. Following administration of granulocyte colony stimulating factor (G-CSF; filgrastim), her neutrophil count increased from 300 to 58,000/microliters, and her dermatosis improved. Pustulosis Palmaris et Plantaris has been described as a representative second lesion of focal infection. Neutropenia may be one cause of Pustulosis Palmaris et Plantaris due to refractory focal infection. In the present case, increase in neutrophils with G-CSF may have improved focal infection, resulting in improvement in refractory Pustulosis Palmaris et Plantaris. More... »

PAGES

453-6

Identifiers

URI

http://scigraph.springernature.com/pub.10.1016/s0925-5710(98)00086-3

DOI

http://dx.doi.org/10.1016/s0925-5710(98)00086-3

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1054664196

PUBMED

https://www.ncbi.nlm.nih.gov/pubmed/9885446


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