Objective: To describe the features of a female patient with a biopsy-proven xanthogranulomatous infiltration of the conjunctiva, limbus and sclera who had an exudative retinal detachment, combined ophthalmic artery and central retinal vein occlusion unilaterally.

Method: A-53-year old otherwise healthy woman presenting with a painful visual loss in her right eye underwent an ophthalmic examination, meticulous systemic work-up and histopathologic assessment.

Results: Ophthalmic examination revealed multiple subconjunctival masses, upper limbal infiltrations, trace cells in the anterior chamber, pale looking posterior fundus, 360 degree scattered retinal hemorrhages and marked exudative retinal detachment in her right eye. Left eye was completely normal.A biopsy taken from one of the subconjunctival masses demonstrated a diffuse infiltration of the histiocytes and this was interpreted as a xanthogranulomatous infiltration with the help of immunohistochemical staining techniques.

Conclusion: Present case is the only reported adult case with xanthogranulomatous-like infiltration of the eyeball featuring both anterior and posterior segment involvement without any concomitant major systemic disturbances.

Download full-text PDF

Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5725586PMC
http://dx.doi.org/10.2174/1874364101711010362DOI Listing

Publication Analysis

Top Keywords

xanthogranulomatous infiltration
12
infiltration conjunctiva
8
conjunctiva limbus
8
limbus sclera
8
combined ophthalmic
8
ophthalmic artery
8
artery central
8
central retinal
8
retinal vein
8
vein occlusion
8

Similar Publications

Xanthogranulomatous inflammation (XGI) is a rare, benign inflammatory condition of unclear pathogenesis, characterised by infiltration and subsequent destruction of normal tissue by lipid-laden macrophages together with lymphocytes and plasma cells. A 56-year-old gentleman was referred to the urology department of our hospital due to concerns that his right testicle felt firmer than his left over the preceding six months. He was investigated and subsequently underwent a right sided orchidectomy.

View Article and Find Full Text PDF
Article Synopsis
  • Xanthogranulomatous inflammation is a rare and chronic inflammatory condition, and its occurrence in the appendix of children, particularly in cases of appendicitis, is extremely uncommon.
  • An 8-year-old boy with Burkitt lymphoma underwent surgery for a mass in his abdomen, where doctors found that his appendix was discolored and abnormal, leading to an appendectomy.
  • The pathology report confirmed xanthogranulomatous appendicitis (XGA), showing distinctive yellow coloration of the appendix and characteristic inflammatory cell infiltration, marking a unique case in medical literature.
View Article and Find Full Text PDF

Xanthogranulomatous osteomyelitis of pubic bone mimicking neoplasm: a case report and literature review.

BMC Musculoskelet Disord

October 2024

Department of Orthopedic Surgery, College of Medicine, Chung-Ang University Hospital, Chung-Ang University, Seoul, Republic of Korea.

Article Synopsis
  • - Xanthogranulomatous osteomyelitis (XO) is a rare bone disease that appears as an osteolytic lesion, and it's crucial to distinguish it from other similar conditions like bone tumors.
  • - A 23-year-old woman presented with pelvic pain and febrile episodes, leading to the discovery of an osteolytic lesion in the pubic bone, which was later confirmed to be caused by an Aspergillus fungal infection after surgical removal.
  • - This case highlights the importance of considering fungal infections in XO cases and suggests that specific antifungal treatments should be included in the management plan, as XO can occur due to such infections despite being predominantly associated with bacteria.
View Article and Find Full Text PDF

Histiocytoses are rare diseases characterised by infiltration of affected organs by myeloid cells with a monocyte or dendritic cell phenotype. Symptoms can range from self-resolving localised forms to multisystemic lesions requiring specific treatment. To demonstrate extremely rare cases of CD68-negative cardiac histiocytosis with expression of SARS-CoV-2 antigen in infiltrate cells.

View Article and Find Full Text PDF

Xanthogranulomatous pyelonephritis (XGP) is an extremely rare, chronic granulomatous inflammatory condition thought to arise secondary to a combination of obstruction, recurrent bacterial infection and an incomplete immune response although the etiology of XGP is more complex. We would like to report a case of XGP occurring in a patient with polycystic kidney disease (PCKD), which has not been previously documented in etiology. A 29-year-old woman presented to our hospital with right upper quadrant pain for 5 days.

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!