Successful Surgical Removal of A Massive Iliopsoas Pseudotumor in a Boy With Mild Hemophilia A

Bobrowski, Alexej; Cseh, Annámaria; Pschibul, Alexander; Schorling, David; Moske-Eick, Olaf; Raedecke, Jochen; Zieger, Barbara

doi:10.1055/a-0586-4514

Cited by 3 publications

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“…2 According to the World Federation of Hemophilia (WFH), it is estimated that about more than 400,000 patients with hemophilia are present worldwide. 3 It has an X-linked pattern of inheritance. Hence, females are mostly carriers of the disorder to the next generation.…”

Section: Introductionmentioning

confidence: 99%

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Female case with misdiagnosis of hemophilia A who underwent total knee arthroplasty: A case report

Bari

Mansouritorghabeh

2022

Clinical Case Reports

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Section: Introductionmentioning

confidence: 99%

“…This disorder can be seen in any part of the world and among all ethnic groups 2 . According to the World Federation of Hemophilia (WFH), it is estimated that about more than 400,000 patients with hemophilia are present worldwide 3 . It has an X‐linked pattern of inheritance.…”

Section: Introductionmentioning

confidence: 99%

Female case with misdiagnosis of hemophilia A who underwent total knee arthroplasty: A case report

Bari

Mansouritorghabeh

2022

Clinical Case Reports

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Pancreas, Adrenal Glands, and Retroperitoneum

Hryhorczuk

Paltiel

2021

Pediatric Ultrasound

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Skull hemophilia pseudotumor: A case report

et al. 2021

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Background In this study, a rare case with hemophilia pseudotumor in the skull was reported. Case presentation The case was a 34-year-old male patient who was admitted to the hospital, with the complaint of dizziness for more than 1 month. The physical examination indicated that the patient was conscious, who could give right answers to the questions. Moreover, there was a bulge on the left frontal-temporal parietal bone. The head CT showed abnormal density lesions on the left frontal-temporal parietal bone, with multiple irregular calcifications within the border. Skull MRI showed a large clump-like mixed signal at the top of the left frontal ridge. After admission, the patient was subjected to complete preoperative preparation and surgical treatment. Neurological navigation was used to determine the extent of skull defect before surgery to make a surgical incision. Clotting factor VIII substitution therapy was used for the intraoperative and postoperative treatments. The lesion was completely removed. Conclusions These results suggest that the skull hemophilia pseudotumor has been rarely seen. According to imaging examination, in combination with family history, the diagnosis can be confirmed. If there is no obvious occupying effect, conservative treatment can be tried. On the contrary, if there is an obvious occupying effect, surgical treatment might be effective, and coagulation factor VIII should be supplemented during the perioperative period.

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Successful Surgical Removal of A Massive Iliopsoas Pseudotumor in a Boy With Mild Hemophilia A

Cited by 3 publications

References 0 publications

Female case with misdiagnosis of hemophilia A who underwent total knee arthroplasty: A case report

Female case with misdiagnosis of hemophilia A who underwent total knee arthroplasty: A case report

Pancreas, Adrenal Glands, and Retroperitoneum

Skull hemophilia pseudotumor: A case report

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