Persistent papular plaques on the face.

Pediatr Dermatol

Christie Clinic Association, Champaign, IL.

Published: September 1989

Download full-text PDF

Source
http://dx.doi.org/10.1111/j.1525-1470.1989.tb00826.xDOI Listing

Publication Analysis

Top Keywords

persistent papular
4
papular plaques
4
plaques face
4
persistent
1
plaques
1
face
1

Similar Publications

Acral Persistent Papular Mucinosis.

Mayo Clin Proc

January 2025

Department of Dermatology, Peking Union Medical College Hospital, State Key Laboratory of Complex Severe and Rare Diseases, Chinese Academy of Medical Science and Peking Union Medical College, National Clinical Research Center for Dermatologic and Immunologic Diseases, Beijing, China. Electronic address:

View Article and Find Full Text PDF
Article Synopsis
  • A 70-year-old patient with a history of bladder cancer treated with BCG developed symptoms like fever, fatigue, and a painful back lesion initially thought to be herpes zoster.
  • Despite antiviral treatment and antibiotics, his condition worsened, leading to further imaging and biopsies that revealed non-caseating granulomas and confirmed disseminated BCG-itis.
  • Treatment with a combination of antibiotics and corticosteroids ultimately resolved the skin lesions and improved the patient's health, highlighting the need for careful diagnosis in similar cases.
View Article and Find Full Text PDF
Article Synopsis
  • * The patient experienced skin rashes and elevated glucagon levels throughout treatment but underwent several surgeries, including pancreatic and liver tumor resections, which led to initial improvements in skin symptoms and glucagon levels post-surgery.
  • * By April 2024, although there were no significant skin symptoms, there was noted progression of liver lesions, indicating that the disease was still advancing despite surgical intervention.
View Article and Find Full Text PDF
Article Synopsis
  • Hereditary C1q deficiency (C1QDef) is a rare genetic disorder that disrupts the complement system and can cause symptoms similar to systemic lupus erythematosus (SLE).
  • A study of 12 genetically confirmed C1QDef patients showed elevated expression of interferon-stimulated genes and high levels of interferon alpha in their blood and cerebrospinal fluid, indicating significant immune dysfunction.
  • Treatment with Janus-kinase inhibitors had mixed results, with one patient improving while others continued to struggle with their condition, highlighting the complexity of managing C1QDef.
View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!