Coexistence of Lupus Nephritis, Ulcerative Colitis, and Communicating Hydrocephalus: A Report of a 21-Year-Old Male

Bushra Ali Khan, Nida Saleem, Danyal Hassan, Shabaz Kiani, Muhammad Haneef

Research output: Contribution to journalArticlepeer-review

18 Downloads (Pure)

Abstract

Systemic lupus erythematosus (SLE) and ulcerative colitis (UC) are multisystem autoimmune disorders that rarely coexist. We report a case history of a 21-year-old male, presenting with bloody diarrhea and, later, diagnosed to have ulcerative colitis on colonic biopsy. There was clinically silent renal impairment leading to end-stage kidney disease requiring hemodialysis possibly secondary to ongoing lupus nephritis as suggested by positive lupus-specific antibodies' detection. Besides this, the diagnosis of lupus associated with early communicating hydrocephalus was made on CT brain findings which clinically responded well to the initiation of immunosuppressive therapy. It is imperative to keep in mind the remote possibility of ulcerative colitis in an SLE patient with gastrointestinal (GI) manifestations. Communicating hydrocephalus is a rare neurological manifestation of SLE leading to seizures and can respond well to the initiation of steroids and immunosuppressants. Therefore, a trial of immunosuppressant medications must be given even in a patient with end-stage renal disease (ESRD) to halter extra renal rare lupus manifestations.

Original languageEnglish
Article number1079300
Number of pages5
JournalCase Reports in Nephrology
Volume2022
DOIs
Publication statusPublished - 2022
Externally publishedYes

Keywords

  • systemic lupus erythematosus (SLE)
  • ulcerative colitis (UC)
  • multisystem autoimmune disorders
  • communicating hydrocephalus
  • hydrocephalus
  • End stage renal disease
  • immunosuppressants

Fingerprint

Dive into the research topics of 'Coexistence of Lupus Nephritis, Ulcerative Colitis, and Communicating Hydrocephalus: A Report of a 21-Year-Old Male'. Together they form a unique fingerprint.

Cite this