Literature DB >> 17261494

Superficial fibromatosis mimicking subcutaneous hematoma: an unusual and difficult diagnosis in a patient with mild hemophilia A.

Yoshihiko Sakurai1, Hiroyuki Sugimoto, Koichi Yoshida, Ichiro Tanaka, Midori Shima, Yasuhito Tanaka, Maiko Takeda, Akitaka Nonomura, Akira Yoshioka.   

Abstract

We present a 16-year-old boy with mild hemophilia A who developed superficial fibromatosis mimicking subcutaneous hematoma of the right upper dorsal region of the foot. This condition is very rare. Hematoma originally developed after the patient sprained the right ankle. Although cast immobilization and replacement therapy with factor VIII (FVIII) concentrates reduced the symptoms, the swelling and pain reappeared in the same region 4 weeks after the cast was removed. A clinical diagnosis of intramuscular hemorrhage was made. Despite readministration of regular FVIII concentrates and cast immobilization, the patient experienced a relapse after removal of the second cast. Magnetic resonance imaging demonstrated a tumor in the extensor digitorum brevis muscle of the right foot with high intensity on T2-weighted images. Marginal excision resulted in symptom resolution. A histopathologic examination of the tissue showed proliferation of fibroblastic cells with abundant collagen bundles. When a mass is found under the skin in hemophilia A patients, an etiology other than bleeding can be overlooked because subcutaneous hemorrhage in limited areas often results in a mass; however, the possibility of rare soft tissue tumors in hemophilia patients should be kept in mind.

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Year:  2007        PMID: 17261494     DOI: 10.1532/IJH97.06084

Source DB:  PubMed          Journal:  Int J Hematol        ISSN: 0925-5710            Impact factor:   2.490


  9 in total

Review 1.  Imaging of musculoskeletal fibromatosis.

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Journal:  Radiographics       Date:  2001 May-Jun       Impact factor: 5.333

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3.  Desmoid tumor arising in a cesarean section scar during pregnancy: monitoring and management.

Authors:  F De Cian; E Delay; R C Rudigoz; D Ranchère; M Rivoire
Journal:  Gynecol Oncol       Date:  1999-10       Impact factor: 5.482

4.  Hereditary gingival fibromatosis with hemophilia B.

Authors:  I Skrinjarić; M Bacić; Z Poje
Journal:  Acta Stomatol Croat       Date:  1983

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Authors:  R Lopez; N Kemalyan; H S Moseley; D Dennis; R M Vetto
Journal:  Am J Surg       Date:  1990-05       Impact factor: 2.565

6.  Fibromatoses of the extremities: clinicopathologic study of 36 cases.

Authors:  A K Mehrotra; S Sheikh; A D Aaron; E Montgomery; J R Goldblum
Journal:  J Surg Oncol       Date:  2000-08       Impact factor: 3.454

7.  Transient hypoplastic anemia caused by primary human parvovirus B19 infection in a previously untreated patient with hemophilia transfused with a plasma-derived, monoclonal antibody-purified factor VIII concentrate.

Authors:  H Matsui; M Sugimoto; S Tsuji; M Shima; J Giddings; A Yoshioka
Journal:  J Pediatr Hematol Oncol       Date:  1999 Jan-Feb       Impact factor: 1.289

Review 8.  Desmopressin in mild hemophilia A: indications, limitations, efficacy, and safety.

Authors:  Stefan Lethagen
Journal:  Semin Thromb Hemost       Date:  2003-02       Impact factor: 4.180

Review 9.  Fibromatosis of the mandible: case report and review of previous publications.

Authors:  D De Santis
Journal:  Br J Oral Maxillofac Surg       Date:  1998-10       Impact factor: 1.651

  9 in total

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