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  February, 2001

Infantile Fibromatosis presenting as a Neck Mass

  I. A Jan, S. Asim, S. Ahmad, T. Barqi, A. A. Chughtai  ( The Children’s Hospital. Pakistan Institute of Medical Sciences PIMS). Islamabad. )
 

Introduction

The fibromatoses are a heterogeneous group of soft tissue lesions sharing common histological features. They are non-metastasizing fibroblastic tumors, which tend to invade locally and may recur after surgical excision. They have been classilied as infantile fibromatoses and adult fibromatoses. Infantile fibrornatoses exclusively occurs in infants and young children under 2 years of age. They usually present as a palpable mass beneath the skin and are most common in the region of axilla, upper arm and shoulders. Scalp and neck are other favored sites. We are presenting a case of infantile fibromatosis in a newborn baby.


Case Report

A 10 days old male baby presented with a firm swelling in the left side of neck. The swelling was present since birth and was progressively increasing in size. The size was 4x5 cm and it was fixed to the deeper structures. CT scan showed a 4.8x5crn soft tissue mass with intracranial extension. Fine needle aspiration cytology of the mass was performed which suggested it to be fibromatoses. kxploration was performed under general anesthesia.

Per-operative findings were a firm mass in the left side of neck invading the left occipital and parietal bones. Dura was luckily spared.

Excision of the mass was performed along with about one centimeter rim of normal bone.

Dura was intact and the bony defect was left as such. Facial nerve was identified by the nerve stimulator and was saved. Postoperative recovery was uneventful and the baby was discharged home in satisfactory condition. Histology of the mass reconfirmed it to be infantile fibromatosis. After nearly three months follow-up there was no evidence of recurrence, as these tumors are notorious for local recurrences.


Discussion

The tibromatoses are a heterogeneous group of soft tissue tumors sharing common histological1. They are fibro-myotibroblastic in origin haying abundance of fibrous and smooth muscle stoma. They are also called myofibromatoses due to the same reason. They are non-metastasizing tumors, which tend to invade locally and have a tendency to recur after surgical excision1,2. They have been c lassi tied as infantile ti brom atoses and adult fihromatoses3. There is lot of controversy about the nomenclature and classification of libromatoses. Infantile fibromatoses includes fibrous hamartoma of infancy. Fibromatosis Coli, Diffuse in fantile Fibromatosis, Juvenile aponeurotic tibroma, digital fibrous tumor of childhood, Congenital Generalized Fibromatosis, Congenital Solitary Fibromatosis, Hereditary gingi va I tibromatosis, Juvenile Nasopharyngeal Angiofibroma and Fibromatosis. Hyalinica Multiplex Juvenilis. Aggressive tibromatosis also called Desmoid tumors are rare childhood tumors1,4,5. They have a familial tendency and are associated with lesion like familial polyposis coli.
Infantile tibromatosis occurs in infants and young children under 2 years of age. They usually present as a palpable mass beneath the skin and are most common in the region of axilla. upper arm and shoulders. Scalp and neck are other favored sites6. Fibromatosis have also been seen in unusual areas like mesentery and abdominal wall7. The lesion are usually solitary but can be multiple. Infantile fibromatosis is locally aggressive and uncapsulated. Boys are more commonly affected than the girls in the ratio of 2:1 to 3: 1. They usually present as a rounded smooth or nodular masses in the subcutaneous tissue. The diagnosis is often easy by the firm to hard consistency of the tumor. They can however easily be confused with haemangiomas. infantile fibrosarcoma and other soft tissue tumors2. Local invasion of the tumors to the adjacent structure occurs early in the course of events. Fixation to the tissue and bone should therefore raise the suspicion of fibromatoses4. Diagnosis can easily be confirmed by tine needle aspiration cytology of the tumors. Invest igations like CT scan and MRI can help in assessing the degree of local invasion. Surgical resection is curative in most cases if an adequate margin of resection of normal tissue is taken4,9. However 10 to 30% cases will have a local recurrence. In one series nearly 75% patients had a recurrence if margin of resections were positive for residual tumor4,10. Therefore a close follow-up is necessary in the these patients. Sponataneous regression of the tumor can occur in few cases2. Some resistant tumors with recurrences may need local radiotherapy or chemotherapy9,11.
Malignant tumors of fibroblastic niyofibroblastic tissue also occur but are much less common1,3.They have also been classified as infantile and adult type of fibrosarcornas. They are recognized histologically by the abundant mitoses and anaplasia. The infantile fibrosarcomas have a less aggressive behavior. Even then the local invasion is early and complete resection is often not possible causing recurrence in nearly 40% of cases. Distant metastasis occurs only in 5% patients. Five years survival of fibrosarcomas is more than 80% however often it is difficult to predict the outcome in these patients.
In summary fibromatoses are rare but interesting tumors in children. They may present at any age. They have an unpredictable behavior and have a tendency of local recurrence. The incidence of local recurrence can however be reduced to minimal if tumor free margins of resection be achieved. Prognosis is very good and even difficult local recurrences can be treated with either wider excision, radiotherapy and chemotherapy.


References

1.Debner Louis P. Soft Tissue, Peritoneum and Reiroperitoncum: In pediatric Surgical Pathology. 2nd Edition. Baltimorc, USA. Williams and Wilkins 1987.pp885-90.
2.Tumors and tumor like condition of the soft tissue Kyriakos Micheal. in Anderson’s Pathology edited by Kissane John M. 9th Edition, St. Louis, The CV Mosby Company., 1971 :pp. I 1844-50.
3.Tumors of soft Tissue by Joseph P. Vacanti, Rober A Cusick in pediatric Surgery 5th ED. Edited by James A. 0 Neil. Mate I Rowe et al. St. Louis. in issouri Mosby Company.. 1989.pp. 1911-4.
4.Faulkner LB. H aidu SI. Kher U. ct al. Pediatric desmoid tumor: retrospective analysis of 63 cases J. Clin. Oncol . 1995:13:2813-8.
5.Kulavlat MN, Karakousis CP. Keanev CM. et al Desmoid tumor: A pleomorphic lesion Emit’. J. Surg. Oncol.. 1999.25:487-97.
6.Perez—Cruet MJ, Burke JM. Weber R. et al Aggressive libromalosis involving the cranial base in children. Neurosurgery., 1998:43:1069-102.
7.Al Jadaam SA. Al Rabeeah A. Mesenteric fibromatosis case report amid litrature review. J. Pediart. Surg . 1999.34 1130-2.
8.Pereira S. Tam E:, Skoog L. Diagnosis of fibromatosis colli by line needle aspiration ( FNA) cytology Cytopathology. 999:10:25-9.
9.Spear MA, Jennings LC. Mankin lii, et al Indi idualizing manageniciti of aggressive fibromatoses Int J. Radial. Oncol. BioL Phvs.. 1998:40:637-45.
10.Baerg J, Murphy JJ. Magee .IF. Fibromatoses clinical and pathological features suggestive of’ recurrences J. Pediatr .Sur g I 1999.34 1112-4.
11.Kamath SS. Parsons jT, Marcus RB, et al Radioihci apy for local conirol of aggiessive fibromatosis lot. J. Radiat. Oncol BioI.Phys. 1996:36:325-8.


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WHO/GOARN Request for technical assistance for Cholera Control in Northern Iraq

Request for assistance

WHO is requesting assistance from GOARN partners to identify the following cholera and diarrhoeal diseases expertise to support the Ministry of Health of Iraq in cholera risk assessment and immediate preparedness activities to improve the health outcomes of the Syrian refugees current living in camps in the Kurdistan region of Iraq.

  • two (2) epidemiologists
  • two (2) clinical management experts
  • one (1) environmental health expert (WATSAN)
  • one (1)laboratory expert

Duration

6 day mission starting 13 June 2014 (this excludes travel time).

Location

Northern Iraq (Kurdistan region).

Language requirements

All candidates must be fluent in English- written, spoken and comprehension. Fluency in Arabic is an asset. Knowledge, abilities and skills All candidates are expected to demonstrate the following

  • Ability to conceptualize and promote innovative strategies and policies.
  • Ability to communicate and write in a clear concise manner, and to develop effective guidelines.
  • Excellent negotiation and interpersonal skills complemented by ability to motivate and lead others and to promote consensus. Tact, discretion and diplomacy
  • Demonstrated ability for project appraisal, project management, monitoring and evaluation and project impact assessment.
  • Ability to work with host governments and their agents, INGOs and national NGOs an advantage.
  • Proven experience of managing a large workload and multiple priorities.
  • Ability to work in difficult conditions.

Support to the mission

WHO/GOARN will cover the travel and per diem (to cover daily expense in the field) expenses for the duration of their mission. GOARN missions do NOT offer salary, consultancy fees or any other form of remuneration.

WHO will provide appropriate logistics support for the field mission. Pre-deployment orientation/training may be required at WHO.

Partners offers of assistance

Partners are requested to reply with offers of assistance, together with CVs and details of the availability of staff for this mission by email to goarn@who.int latest by 30 May 2014. Details of all offers from partners and eventual deployments will be maintained on the GOARN SharePoint.

Operational Contacts

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