Desmoid tumor

A desmoid tumor (DT) is a benign, locally invasive soft tissue tumor associated with a high recurrence rate but with no metastatic potential.

Fibroma

Benign tumors that are composed of fibrous or connective tissue. They can grow in all organs, arising from mesenchyme tissue. The term \"fibroblastic\" or \"fibromatous\" is used to describe tumors of the fibrous connective tissue. When the term fibroma is used without modifier, it is usually considered benign, with the term fibrosarcoma reserved for malignant tumors.


Total: 25

                      


(per page)
PMID (PMCID)
29517699
(5882433)
FEMALE Adult
Misdiagnosis of aggressive fibromatosis of the abdominal wall: A case report and literature review.
Liu X, Zong S, Cui Y, Yue Y.
Medicine (Baltimore). 2018;97(10):e9925.
Aggressive fibromatosis (AF) of abdominal wall is also called desmoid tumor, ligament tumor, fibrous tissue tumor hyperplasia, tendon membrane fibroma or soft tissue ligament fibroma, etc.
29517699
(5882433)
FEMALE Adult
Misdiagnosis of aggressive fibromatosis of the abdominal wall: A case report and literature review.
Liu X, Zong S, Cui Y, Yue Y.
Medicine (Baltimore). 2018;97(10):e9925.
Aggressive fibromatosis (AF) of abdominal wall is also called desmoid tumor, ligament tumor, fibrous tissue tumor hyperplasia, tendon membrane fibroma or soft tissue ligament fibroma, etc.
29517699
(5882433)
FEMALE Adult
Misdiagnosis of aggressive fibromatosis of the abdominal wall: A case report and literature review.
Liu X, Zong S, Cui Y, Yue Y.
Medicine (Baltimore). 2018;97(10):e9925.
Aggressive fibromatosis (AF) of abdominal wall is also called desmoid tumor, ligament tumor, fibrous tissue tumor hyperplasia, tendon membrane fibroma or soft tissue ligament fibroma, etc.
29517699
(5882433)
FEMALE Adult
Misdiagnosis of aggressive fibromatosis of the abdominal wall: A case report and literature review.
Liu X, Zong S, Cui Y, Yue Y.
Medicine (Baltimore). 2018;97(10):e9925.
Aggressive fibromatosis (AF) of abdominal wall is also called desmoid tumor, ligament tumor, fibrous tissue tumor hyperplasia, tendon membrane fibroma or soft tissue ligament fibroma, etc.
26893769
OTHER
Treatment and functional result of desmoplastic fibroma with repeated recurrences in the forearm: A case report.
Rui J, Guan W, Gu Y, Lao J.
Oncol Lett. 2016;11(2):1506-1508.
Desmoplastic fibroma, alternatively known as aggressive fibromatosis or desmoid tumors, occurs in the form of benign locally aggressive tumors that possess a high rate of recurrence.
26893769
OTHER
Treatment and functional result of desmoplastic fibroma with repeated recurrences in the forearm: A case report.
Rui J, Guan W, Gu Y, Lao J.
Oncol Lett. 2016;11(2):1506-1508.
Desmoplastic fibroma, alternatively known as aggressive fibromatosis or desmoid tumors, occurs in the form of benign locally aggressive tumors that possess a high rate of recurrence.
25113037
FEMALE Young Adult
Desmoplastic fibroma of the mandible: a series of three cases and review of literature.
Woods TR, Cohen DM, Islam MN, Rawal Y, Bhattacharyya I.
Head Neck Pathol. 2015;9(2):196-204.
The desmoplastic fibroma (DF) is a rare, fibroblastic lesion of bone that histologically resembles the desmoid tumor of soft tissue.
25074465
MIXED_SAMPLE Infant
Identification of previously unrecognized FAP in children with Gardner fibroma.
Vieira J, Pinto C, Afonso M, do Bom Sucesso M, Lopes P, Pinheiro M, Veiga I, Henrique R, Teixeira MR.
Eur J Hum Genet. 2015;23(5):715-8.
Fibromatous soft tissue lesions, namely desmoid-type fibromatosis and Gardner fibroma, may occur sporadically or as a result of inherited predisposition (as part of familial adenomatous polyposis, FAP).
25074465
MIXED_SAMPLE Infant
Identification of previously unrecognized FAP in children with Gardner fibroma.
Vieira J, Pinto C, Afonso M, do Bom Sucesso M, Lopes P, Pinheiro M, Veiga I, Henrique R, Teixeira MR.
Eur J Hum Genet. 2015;23(5):715-8.
Whereas desmoid-type fibromatosis often present 946-catenin overexpression (by activating CTNNB1 somatic variants or APC biallelic inactivation), the pathogenetic mechanisms in Gardner fibroma are unknown.
24265574
(3835646)
MIXED_SAMPLE
Desmoplastic fibroma of bone in a toe: radiographic and MRI findings.
Kim OH, Kim SJ, Kim JY, Ryu JH, Choo HJ, Lee SJ, Lee IS, Suh KJ.
Korean J Radiol. 2013;14(6):963-7.
Desmoplastic fibroma is a rare benign primary bone tumor that is histologically similar to the soft tissue desmoid tumor.
23459513
(3583030)
OTHER
Desmoplastic fibroma: a case report with three years of clinical and radiographic observation and review of the literature.
Nedopil A, Raab P, Rudert M.
Open Orthop J. 2013;8:40-6.
Histologically and biologically, desmoplastic fibroma mimics extra-abdominal desmoid tumor of soft tissue.
21977480
(3174467)
OTHER
Central odontogenic fibroma: a case report.
Nah KS.
Imaging Sci Dent. 2011;41(2):85-8.
Since the present case showed a multilocular radiolucency with partially ill-defined border between the right mandibular condyle and the distal root of the right mandibular third molar, differential diagnosis involved a wide range of pathosis from benign lesions like ameoloblastic fibroma and odontogenic myxoma to more aggressive lesions such as desmoplastic fibroma, juvenile aggressive fibromatosis, or fibrosarcoma.
21977480
(3174467)
OTHER
Central odontogenic fibroma: a case report.
Nah KS.
Imaging Sci Dent. 2011;41(2):85-8.
Since the present case showed a multilocular radiolucency with partially ill-defined border between the right mandibular condyle and the distal root of the right mandibular third molar, differential diagnosis involved a wide range of pathosis from benign lesions like ameoloblastic fibroma and odontogenic myxoma to more aggressive lesions such as desmoplastic fibroma, juvenile aggressive fibromatosis, or fibrosarcoma.
20063100
MIXED_SAMPLE Adult
[Gardner fibroma: case report and discussion of a new soft tissue tumor entity].
Lanckohr C, Debiec-Rychter M, Muller O, Homann HH, Lehnhardt M, Herter P, Kuhnen C.
Pathologe. 2010;31(2):97-105.
The case of a 13-year-old male patient with Gardner fibroma and osteoma and multicentric desmoid type fibromatosis in his mother is presented with detection of a (heterozygotic) germline mutation of the APC gene leading to a de novo stop codon (deletion of base pairs 5033-5036).
20063100
MIXED_SAMPLE Adult
[Gardner fibroma: case report and discussion of a new soft tissue tumor entity].
Lanckohr C, Debiec-Rychter M, Muller O, Homann HH, Lehnhardt M, Herter P, Kuhnen C.
Pathologe. 2010;31(2):97-105.
Gardner fibroma in children and young adults may serve as an indicator lesion for familial adenomatous polyposis (FAP), Gardner syndrome, a familial desmoid type fibromatosis without other manifestations of APC or a new APC gene mutation.
16498294
MIXED_SAMPLE Middle Aged
[Desmoplastic fibroma of the rib: two case reports].
Ayadi-Kaddour A, Ben Slama S, Braham E, Abid L, Ismail O, Smati B, Djilani H, El Mezni F.
Ann Pathol. 2005;25(5):398-401.
Desmoplastic fibroma is a very rare primary tumor of bone, closely related to aggressive fibromatosis of soft tissue.
16553001
MIXED_SAMPLE Adult
[Desmoplastic fibroma or bone desmoid tumor: two cases].
Vaz G, Richard A, Guyen O, Bejui-Hugues J, Carret JP.
Rev Chir Orthop Reparatrice Appar Mot. 2005;91(8):782-7.
[Desmoplastic fibroma or bone desmoid tumor: two cases].
12652337
MALE
Desmoid tumor of bone with enchondromatous nodules, mistaken for chondrosarcoma.
Bahk WJ, Kang YK, Lee AH, Mirra JM.
Skeletal Radiol. 2003;32(4):223-6.
Desmoid tumor of bone, also termed desmoplastic fibroma or aggressive fibromatosis, is a rare, locally aggressive fibroblastic tumor.
12652337
MALE
Desmoid tumor of bone with enchondromatous nodules, mistaken for chondrosarcoma.
Bahk WJ, Kang YK, Lee AH, Mirra JM.
Skeletal Radiol. 2003;32(4):223-6.
Desmoid tumor of bone, also termed desmoplastic fibroma or aggressive fibromatosis, is a rare, locally aggressive fibroblastic tumor.
12033964
MALE
Desmoplastic fibroma of the rib.
Barbashina V, Karabakhtsian R, Aisner S, Bolanowski P, Patterson F, Hameed M.
Arch Pathol Lab Med. 2002;126(6):721-2.
Desmoplastic fibroma is a very rare primary tumor of bone, closely related to aggressive fibromatosis of soft tissue.