Multifocal bilateral xanthogranulomatous osteomyelitis.

Indian J Orthop

Department of Orthopedics, S. M. S. Hospital, Jaipur, India.

Published: August 2015

Xanthogranulomatous osteomyelitis is a rare chronic inflammatory disorder which clinically resembles bone tumor. It is characterized histologically by the presence of a large number of foamy histiocytes admixed with lymphocytes and plasma cells. Xanthogranulomatous inflammation can involve any organ, with kidneys and gall bladder being the worst affected. Only anecdotal cases of osteomyelitis have been reported in the past with scant medical literature. However, all the earlier reported cases, except one, were unifocal lesions. The authors present a case of multifocal xanthogranulomatous osteomyelitis involving the left medial malleoli, left talus and the right cuboid bones.

Download full-text PDF

Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4510806PMC
http://dx.doi.org/10.4103/0019-5413.159682DOI Listing

Publication Analysis

Top Keywords

xanthogranulomatous osteomyelitis
12
multifocal bilateral
4
xanthogranulomatous
4
bilateral xanthogranulomatous
4
osteomyelitis
4
osteomyelitis xanthogranulomatous
4
osteomyelitis rare
4
rare chronic
4
chronic inflammatory
4
inflammatory disorder
4

Similar Publications

The case report discusses xanthogranulomatous osteomyelitis, a rare inflammatory bone condition that can resemble malignancy on imaging studies. The report details a case of a 42-year-old woman with left leg pain, swelling, and redness lasting 4 months. Imaging revealed a lytic lesion in the left tibia with endosteal erosion, and MRI showed extraosseous soft tissue extension.

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
Article Synopsis
  • Xanthogranulomatous osteomyelitis (XO) is a rare inflammatory bone disease marked by cholesterol-filled foam macrophages and other immune cells.
  • A case study describes a 41-year-old man with end-stage renal disease who developed a chest wall mass two weeks before hospital admission, showing significant osteolytic lesions on imaging.
  • A surgical resection confirmed the XO diagnosis through pathological examination, highlighting that XO can occur after kidney transplantation.
View Article and Find Full Text PDF

Sclerosing osteomyelitis of Garré is a rare inflammatory pathology characterized by cortical thickening and loss of the medullary canal. Typically, this pathology affects the mandible. However, the involvement of long bones, such as the femur and tibia, is also possible.

View Article and Find Full Text PDF

Xanthogranulomatous osteomyelitis is a rare chronic inflammatory disorder. Until now, it has only been reported in long bones. To the best of our knowledge, it has never been reported in temporal bone.

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!