Cargando…
Coexistence of Lupus Nephritis, Ulcerative Colitis, and Communicating Hydrocephalus: A Report of a 21-Year-Old Male
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 ren...
Autores principales: | , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8843975/ https://www.ncbi.nlm.nih.gov/pubmed/35178259 http://dx.doi.org/10.1155/2022/1079300 |
_version_ | 1784651383132127232 |
---|---|
author | Khan, Bushra Ali Saleem, Nida Hassan, Danyal Kiani, Shabaz Haneef, Muhammad |
author_facet | Khan, Bushra Ali Saleem, Nida Hassan, Danyal Kiani, Shabaz Haneef, Muhammad |
author_sort | Khan, Bushra Ali |
collection | PubMed |
description | 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. |
format | Online Article Text |
id | pubmed-8843975 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Hindawi |
record_format | MEDLINE/PubMed |
spelling | pubmed-88439752022-02-16 Coexistence of Lupus Nephritis, Ulcerative Colitis, and Communicating Hydrocephalus: A Report of a 21-Year-Old Male Khan, Bushra Ali Saleem, Nida Hassan, Danyal Kiani, Shabaz Haneef, Muhammad Case Rep Nephrol Case Report 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. Hindawi 2022-02-04 /pmc/articles/PMC8843975/ /pubmed/35178259 http://dx.doi.org/10.1155/2022/1079300 Text en Copyright © 2022 Bushra Ali Khan et al. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Case Report Khan, Bushra Ali Saleem, Nida Hassan, Danyal Kiani, Shabaz Haneef, Muhammad Coexistence of Lupus Nephritis, Ulcerative Colitis, and Communicating Hydrocephalus: A Report of a 21-Year-Old Male |
title | Coexistence of Lupus Nephritis, Ulcerative Colitis, and Communicating Hydrocephalus: A Report of a 21-Year-Old Male |
title_full | Coexistence of Lupus Nephritis, Ulcerative Colitis, and Communicating Hydrocephalus: A Report of a 21-Year-Old Male |
title_fullStr | Coexistence of Lupus Nephritis, Ulcerative Colitis, and Communicating Hydrocephalus: A Report of a 21-Year-Old Male |
title_full_unstemmed | Coexistence of Lupus Nephritis, Ulcerative Colitis, and Communicating Hydrocephalus: A Report of a 21-Year-Old Male |
title_short | Coexistence of Lupus Nephritis, Ulcerative Colitis, and Communicating Hydrocephalus: A Report of a 21-Year-Old Male |
title_sort | coexistence of lupus nephritis, ulcerative colitis, and communicating hydrocephalus: a report of a 21-year-old male |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8843975/ https://www.ncbi.nlm.nih.gov/pubmed/35178259 http://dx.doi.org/10.1155/2022/1079300 |
work_keys_str_mv | AT khanbushraali coexistenceoflupusnephritisulcerativecolitisandcommunicatinghydrocephalusareportofa21yearoldmale AT saleemnida coexistenceoflupusnephritisulcerativecolitisandcommunicatinghydrocephalusareportofa21yearoldmale AT hassandanyal coexistenceoflupusnephritisulcerativecolitisandcommunicatinghydrocephalusareportofa21yearoldmale AT kianishabaz coexistenceoflupusnephritisulcerativecolitisandcommunicatinghydrocephalusareportofa21yearoldmale AT haneefmuhammad coexistenceoflupusnephritisulcerativecolitisandcommunicatinghydrocephalusareportofa21yearoldmale |