1.Collagenous Fibroma (Desmoplastic Fibroblastoma) .
Muharrem DAGLI ; Adil ERYILMAZ ; Aydin ACAR ; Sezer KULACOGLU ; Halit AKMANSU
Yonsei Medical Journal 2004;45(5):941-943
A Collagenous Fibroma (Desmoplastic Fibroblastoma) is a rare, benign, slowly growing, fibroblastic, soft tissue lesion. Here, the case of a 28-year-old woman, who presented with a 1-year history of a slowly growing painless mass in the right anterior aspect of her neck, is described. This type of tumor was first described by Evans in 1995, and named as a Desmoplastic fibroblastoma but was renamed, by Nielsen in 1996 as a Collagenous Fibroma. This type of tumor is frequently reported in men with a mean age at occurance of 50 years. Clinically, a Collagenous fibroma presents as a firm, well-circumscribed subcutaneous, or intramuscular, painless mass of long duration. They are mostly located in the neck and extremities. The tumors range in size from 1 to 20 cm and predominantly occurs within the subcutaneous tissue, but fascial and skeletal muscle involvement is common. The treatment of a Collagenous Fibroma is a total surgical excision. No tumor recurrence has been reported the literature during the follow-up period and no tumor recurrence was observed in our case at the 1-year follow-up.
Adult
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Female
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Fibroma, Desmoplastic/*pathology
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Humans
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Soft Tissue Neoplasms/*pathology
3.Desmoplastic Fibroma of Bone in a Toe: Radiographic and MRI Findings.
Ok Hwa KIM ; Seon Jeong KIM ; Ji Yeon KIM ; Ji Hwa RYU ; Hye Jung CHOO ; Sun Joo LEE ; In Sook LEE ; Kyung Jin SUH
Korean Journal of Radiology 2013;14(6):963-967
Desmoplastic fibroma is a rare benign primary bone tumor that is histologically similar to the soft tissue desmoid tumor. It most often involves the mandible, large long bone or iliac bone. Desmoplastic fibroma in a toe has been extremely rarely reported. Authors report a rare case of desmoplastic fibroma of bone occurring in the distal phalanx of a foot, with descriptions of the radiographic and MRI findings, correlation of the radiologic and pathologic findings, and discussion on the differential diagnosis of the tumor.
Adolescent
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Bone Neoplasms/*diagnosis
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Diagnosis, Differential
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Female
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Fibroma, Desmoplastic/*diagnosis
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Humans
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Magnetic Resonance Imaging
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Male
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Toes/*pathology
4.Imaging Findings Of Desmoplastic Fibroma Rarely Involving The Clavicle: Case Report.
Dong Min KANG ; Seon Kwan JUHNG ; Young Jun SOHN ; Hun Soo KIM
Korean Journal of Radiology 2014;15(1):130-133
Desmoplastic fibroma of bone is a rare locally aggressive, but non-metastatic tumor. In this case report, we present a desmoplastic fibroma in an unusual location, the clavicle. Desmoplastic fibroma involving the clavicle is extremely rare, with only 2 reported cases before 1985. We report the imaging findings of a desmoplastic fibroma of the clavicle with a review of the relevant literature.
Adult
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Bone Neoplasms/*diagnosis/pathology/radiography
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*Clavicle/pathology/radiography
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Fibroma, Desmoplastic/*diagnosis/pathology/radiography
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Humans
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Magnetic Resonance Imaging
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Male
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Tomography, X-Ray Computed
5.Surgical treatment for desmoplastic fibroma of bone.
Jia-Kai ZHANG ; Qing-Jiang PANG
China Journal of Orthopaedics and Traumatology 2013;26(8):696-699
OBJECTIVETo discuss clinical effects of surgical treatment for desmoplastic fibroma of bone.
METHODSBetween June 2000 and June 2010, 15 cases of desmoplastic fibroma were treated by surgical operation including 4 males and 7 females with an average age of 39 years old (ranged from 18 to 64 years old). The site of tumor was proximal femur in 4 cases, distal femur in 3, distal tibia in 2, proximal humerus in 1, distal humerus in 1, scapula in 1, pelvic in 2, manubrium of sternum in 1. The simple intralesional curettage was performed in 1 case. The other 14 cases were divided into two groups, 7 cases had an aggressive curettage with inactivation and the last 7 cases had a wide resection. Recurrence condition were observed after operation. The function was valuated in two groups after the operation according to Enneking's standard.
RESULTSThe mean duration of follow-up was 56 months (ranged, 18 to 132 months). Two cases recurred, but no metastasis. The patient with simple intralesional curettage recurreed, 1 of the 7 patients with a wide resection recurred. The recurrence rate was 13.3% (2/15). There was no recurrence in the group with an aggressive curettage with inactivation. According to Enneking's standard, Enneking scoring was 21.6 +/- 3.8 in the group with a wide resection and 28.3 +/- 1.3 in another group, The results were excellent in 2 cases and good in 5 in the group with a wide resection, excellent in 7 in the other group.
CONCLUSIONThe aggressive curettage with inactivation has better functional recovery than the wide resection,and it should be chosen when the lesion is small or located in an area where reconstruction is difficult.
Adolescent ; Adult ; Bone Neoplasms ; pathology ; surgery ; Female ; Fibroma, Desmoplastic ; pathology ; surgery ; Humans ; Male ; Middle Aged ; Neoplasm Recurrence, Local ; epidemiology ; Young Adult