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| http://dx.doi.org/10.1136/bcr-2013-008731 | DOI Listing |
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Spontaneous resolution and bone regeneration in hemophilic pseudotumor: A rare case report and literature review.
Spec Care Dentist
November 2024
Department of Medicine & In-charge Hemophilia Day Care Centre, Lok Nayak Hospital and Maulana Azad Medical College, New Delhi, India.
Aim: Hemophilic pseudotumor (HP) is a very rare complication of hemophilia seen in only 1-2% of the cases. Although it is much more common in long bones, pelvis and small bones of hands and feet and very rarely involving jaw bones.
Method And Result: In the present case, the presence of a rare hemophilic pseudotumor of the mandible with the positive history of Hemophilia B justifies that the history, clinical and radiological examinations were sufficient to arrive at conclusive diagnosis precluding invasive diagnostic procedures such as biopsy hence avoiding the risk of hemorrhage, infection, or fistula.
Hemophilic pseudotumor in the bilateral forearms: a unique case report.
Skeletal Radiol
July 2024
University of Texas Medical Branch, Galveston, USA.
Hemophilic pseudotumor (HP) is a rarely encountered cystic mass that forms as a result of repeated bleeding from extra-articular soft tissues. HP cases have been previously documented in several locations in the body, most commonly in the femur and pelvis. To date, no upper extremity case involving the bilateral forearms has been reported.
View Article and Find Full Text PDFSurgical treatment for pelvic haemophilic pseudotumour: a retrospective analysis of 21 cases.
EClinicalMedicine
March 2024
Department of Orthopedics, Peking Union Medical College Hospital, Beijing 100730, People's Republic of China.
Background: Due to the rarity of pelvic haemophilic pseudotumour (PHPT) and demanding surgical technique for PHPT excision, no study reports the mid-term follow-up outcomes of surgical treatment of PHPT in a relatively large cohort. PHPT with varying degrees of bony pelvic involvement and infection status necessitates different operative procedures, yet there is currently no classification system for PHPT based on surgical practice.
Methods: The study was conducted between June 25, 2004 and July 18, 2023, in Peking Union Medical College Hospital and Nanfang Hospital in China.
Nasal hemophilic pseudotumor in a 2-year-old with recurrent epistaxis: a case report and review of the literature.
J Surg Case Rep
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Department of Otolaryngology-Head & Neck Surgery, King Faisal Specialist Hospital and Research Center, Jeddah, Saudi Arabia.
Hemophilic pseudotumor is a rare, yet dangerous complication of hemophilia. It has been reported previously at sites prone to recurrent trauma like long bones and pelvis. However, in the field of otorhinolaryngology, few cases are reported and therefore there is no established protocol for management.
View Article and Find Full Text PDFGiant pelvic haemophilic pseudotumor.
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Department of Orthopaedics, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China.
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