Acta Scientific Medical Sciences (ISSN: 2582-0931)

Case Report Volume 4 Issue 3

My fibroma Infantile Solitary: About A Case

Fatima Zahra Agharbi

Tétouan Civil Hospital, Tétouan, Morocco

*Corresponding Author: Fatima zahra Agharbi, Tétouan Civil Hospital, Tétouan, Morocco.

Received: January 02, 2020; Published: February 08, 2020

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Abstract

  Infantile myofibromatosis (ILM) described by Enzinger in 1981 is the most common childhood fibromatosis. It consists of a benign proliferation of fibroblasts and myofibroblasts. There are three forms. Solitary MFI, the most common type, characterized by isolated skin, bone or soft tissue injury; multiple MFI represented by several locations and generalized MFI with visceral involvement. The morphological characters are identical whatever the location. The histological diagnosis is based on the identification of a double component, myofibroblast fasciculate at the periphery and hemangiopericytomas at the centre, which expresses smooth muscle actin. There is usually no atypia or mitosis, but there can be observed images of intravascular extensions in the centre. In the solitary form, the prognosis of MFI is good but it is often fatal in cases of visceral involvement. The reported case concerns a 4-year-old child who has had a left inguinal nodule since the age of 1, whose histological study after surgical excision has led to the diagnosis of myofibroma.

Keywords: Myofibroma; Myofibromatosis; Localized; Multiple; Generalised

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References

  1. C Giannakopoulou. “Infantile myofibromatosis: a case study and review of literature”. The Journal of Dermatology 26.9 (1999): 595-598. 
  2. EB Chung and FM Enzinger. “Infanti the myofibromatosis”. Cancer 48.8 (1981): 1807-1818. 
  3. SW Weiss and JR Goldblum. “Enzinger and Weiss’s Soft tissue tumors”. 4th ed. St. Louis: Mosby (2001): 357-360. 
  4. Stanford D and Rogers M. “Dermatological presentations of infantile myofibromatosis: a review of 27 cases”. Australasian Journal of Dermatology 41.3 (2000): 156-161. 
  5. T Hasegawa., et al. “Solitary infantile myofibromatosis of bone”. The American Journal of Surgical Pathology 17.3 (1993): 308-313. 
  6. S Ijima., et al. “Solitary form of infantile myofibromatosis: a histologic, immunohistochemical, and electronmicroscopic study of a regressing tumor over a 20-month period”. The American Journal of Dermatopathology 21.4 (1999): 375-380. 
  7. SF Hogan and JR Salassa. “Recurrent adult myofibromatosis. A case report”. The American Journal of Dermatopathology 97.6 (1992): 810-814. 
  8. DT Netsche. “Infantile myofibromatosis: case report of a solitary hand lesion with emphasis on differential diagnosis and management”. Annals of Plastic Surgery 46.1 (2001): 62-67. 
  9. NS Goldberg., et al. “Infantile myofibromatosis: a review of clinicopathology with perspectives on new treatment choices”. Pediatric Dermatology 5.1 (1988): 37-46. 
  10. N Loundon. “Head and neck infantile myofibromatosis: a report of three cases”. International Journal of Pediatric Otorhinolaryngology 51.3 (1999): 181-186. 
  11. B Raney., et al. “Nonsurgical management of children with recurrent or unresectable fibromatosis”. Pediatrics 79.3 (1987): 394-398. 
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Citation

Citation: Fatima Zahra Agharbi. “My fibroma Infantile Solitary: About A Case". Acta Scientific Medical Sciences 4.3 (2020): 01-02.



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