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.



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Narrow down the case reports



Total: 405 (papers)

  


(per page)
Matched Phenotype  Gene  Mutation  MeSH
Rank
(Similarity)
PMID
(PMCID)
15
(23.3%)
7850535
Radical forequarter amputation with hemithoracectomy and free extended forearm flap: technical and physiologic considerations.
Kuhn JA, Wagman LD, Lorant JA, Grannis FW, Dunst M, Dougherty WR, Jacobs DI.
Ann Surg Oncol. 1994;1(4):353-9.
Fever Scoliosis
Adult Fibromatosis, Aggressive Forearm Homo sapiens Male Neoplasm Recurrence, Local Pneumonectomy Respiration, Artificial Surgical Flaps Thoracic Neoplasms Thoracotomy
15
(23.3%)
7850046
Techniques in the composite reconstruction of extensive thoracoabdominal tumor resections.
Kao CC, Rand RP, Stridde BC, Marchioro TL.
J Am Coll Surg. 1995;180(2):146-9.
Rigidity Thoracoabdominal wall defect
Abdominal Neoplasms Adult Chondrosarcoma Feasibility Studies Fibromatosis, Aggressive Homo sapiens Male Methylmethacrylates Polypropylenes Surgical Flaps Surgical Mesh Thoracic Neoplasms
15
(23.3%)
7730568
[Fibromatosis found during prenatal ultrasonography].
Col JY, Vannier JP, Chabrolle JP, Brottier C.
J Gynecol Obstet Biol Reprod (Paris). 1995;24(1):52-6.
Scoliosis
Adult Females Fetal Diseases Fibromatosis, Aggressive Homo sapiens Magnetic Resonance Imaging Pregnancy Ultrasonography, Prenatal
15
(23.3%)
6612196
[An unusual cause of sciatica: soft tissue desmoid tumor. Apropos of 2 cases].
Bregeon C, Renier JC, Pidhorz L, Francois J, Cardi S, Maze H.
Rev Rhum Mal Osteoartic. 1983;50(6):427-34.
Sciatica
Adult Buttocks Females Homo sapiens Neoplasm Recurrence, Local Sciatica Soft Tissue Neoplasms X-Ray Computed Tomography
25
(21.2%)
25971832
(6074574)
Melorheostosis mimicking synovial osteochondromatosis.
Wadhwa V, Chhabra A, Samet JD.
Ann Saudi Med. 2014;34(6):547-50.
Nephrotic syndrome Osteopoikilosis
Chondromatosis, Synovial Differential Diagnosis Females Homo sapiens Magnetic Resonance Imaging Melorheostosis Middle Aged
25
(21.2%)
25324480
A large deletion of chromosome 5q22.1-22.2 associated with sparse type of familial adenomatous polyposis: report of a case.
Yamaguchi T, Koizumi K, Arai M, Tamura K, Iijima T, Horiguchi S, Miyaki M.
Jpn J Clin Oncol. 2014;44(12):1243-7.
Osteoma
Adenomatous Polyposis Coli Adult Chromosome Deletion Chromosomes, Human, Pair 5 Fluorescent in Situ Hybridization Homo sapiens Male
25
(21.2%)
24579232
Pelvic deformity secondary to tensor fascia lata tightness associated with desmoid tumor.
Dhamangaonkar AC, Joshi D, Goregaonkar AB, Phalak M.
Orthopedics. 2013;36(12):e1563-6.
Flexion contracture
Adult Fibromatosis, Aggressive Hip Contracture Hip Joint Homo sapiens Joint Deformities, Acquired Male
25
(21.2%)
23268029
[Hepatocellular adenocarcinoma with fundic gland polyposis in adolescents associated with ileal J -pouch anal anastomosis for familial adenomatous polyposis].
Tomita R, Fujisaki S, Sakurai K, Park E, Shibata M.
Gan To Kagaku Ryoho. 2012;39(12):2219-21.
Osteoma
Adenomatous Polyposis Coli Colonic Pouches Hepatocellular Adenoma Homo sapiens Male Stomach Neoplasms Young Adult
25
(21.2%)
20063100
[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.
Fibroma Osteoma
Adult Biomarkers, Tumor Chromosome Deletion Chromosomes, Human, Pair 5 Codon, Terminator DNA Mutational Analysis Females Fibromatosis, Aggressive Fluorescent in Situ Hybridization Follow-Up Studies Gardner Syndrome Genetic Carrier Screening Germ-Line Mutation Homo sapiens Loss of Heterozygosity Male Neoplasm Recurrence, Local Osteoma Soft Tissue Neoplasms Young Adult
25
(21.2%)
15111819
Benign osteoma with Gardner syndrome: review of the literature and report of a case.
Bilkay U, Erdem O, Ozek C, Helvaci E, Kilic K, Ertan Y, Gurler T.
J Craniofac Surg. 2004;15(3):506-9.
Neoplasm Osteoma
Gardner Syndrome Homo sapiens Male Mandibular Neoplasms Maxillary Neoplasms Middle Aged Osteoma Skull Neoplasms
        

Phenotype(s) retrieved from Orphanet

    Total: 20

HPO ID Term Frequency
HP:0001482 Subcutaneous nodule Very frequent (99-80%)
HP:0003011 Abnormality of the musculature Very frequent (99-80%)
HP:0004298 Abnormality of the abdominal wall Very frequent (99-80%)
HP:0010614 Fibroma Very frequent (99-80%)
HP:0100245 Desmoid tumors Very frequent (99-80%)
HP:0002024 Malabsorption Frequent (79-30%)
HP:0002027 Abdominal pain Frequent (79-30%)
HP:0003326 Myalgia Frequent (79-30%)
HP:0007703 Abnormality of retinal pigmentation Frequent (79-30%)
HP:0200008 Intestinal polyposis Frequent (79-30%)
HP:0000126 Hydronephrosis Occasional (29-5%)
HP:0001376 Limitation of joint mobility Occasional (29-5%)
HP:0002239 Gastrointestinal hemorrhage Occasional (29-5%)
HP:0002797 Osteolysis Occasional (29-5%)
HP:0002829 Arthralgia Occasional (29-5%)
HP:0005214 Intestinal obstruction Occasional (29-5%)
HP:0008069 Neoplasm of the skin Occasional (29-5%)
HP:0010935 Abnormality of the upper urinary tract Occasional (29-5%)
HP:0100749 Chest pain Occasional (29-5%)
HP:0100806 Sepsis Occasional (29-5%)


Phenotype(s) retrieved from case reports

    Total: 82

HPO ID Term # of case reports
HP:0002664 Neoplasm 61
HP:0010614 Fibroma 17
HP:0100242 Sarcoma 14
HP:0030731 Carcinoma 13
HP:0025615 Abscess 9
HP:0031500 Abdominal mass 9
HP:0012032 Lipoma 8
HP:0003002 Breast carcinoma 6
HP:0006000 Ureteral obstruction 5
HP:0010866 Abdominal wall defect 5
HP:0200040 Epidermoid cyst 5
HP:0001028 Hemangioma 4
HP:0003003 Colon cancer 4
HP:0005200 Retroperitoneal fibrosis 4
HP:0100008 Schwannoma 4
HP:0000718 Aggressive behavior 3
HP:0002027 Abdominal pain 3
HP:0002835 Aspiration 3
HP:0002860 Squamous cell carcinoma 3
HP:0031459 Soft tissue neoplasm 3
HP:0100246 Osteoma 3
HP:0100699 Scarring 3
HP:0100790 Hernia 3
HP:0000131 Uterine leiomyoma 2
HP:0002797 Osteolysis 2
HP:0012315 Histiocytoma 2
HP:0000016 Urinary retention 1
HP:0000100 Nephrotic syndrome 1
HP:0000126 Hydronephrosis 1
HP:0000138 Ovarian cyst 1
HP:0000211 Trismus 1
HP:0000488 Retinopathy 1
HP:0000822 Hypertension 1
HP:0000836 Hyperthyroidism 1
HP:0000873 Diabetes insipidus 1
HP:0001067 Neurofibromas 1
HP:0001289 Confusion 1
HP:0001537 Umbilical hernia 1
HP:0001880 Eosinophilia 1
HP:0001903 Anemia 1
HP:0002014 Diarrhea 1
HP:0002015 Dysphagia 1
HP:0002094 Dyspnea 1
HP:0002206 Pulmonary fibrosis 1
HP:0002586 Peritonitis 1
HP:0002650 Scoliosis 1
HP:0002666 Pheochromocytoma 1
HP:0002861 Melanoma 1
HP:0003031 Ulnar bowing 1
HP:0003273 Hip contracture 1
HP:0003302 Spondylolisthesis 1
HP:0003326 Myalgia 1
HP:0003419 Low back pain 1
HP:0003470 Paralysis 1
HP:0003761 Calcinosis 1
HP:0003764 Nevus 1
HP:0004783 Duodenal polyposis 1
HP:0004872 Incisional hernia 1
HP:0005257 Thoracic hypoplasia 1
HP:0005266 Intestinal polyp 1
HP:0006725 Pancreatic adenocarcinoma 1
HP:0007687 Unilateral ptosis 1
HP:0008443 Spinal deformities 1
HP:0009937 Facial hirsutism 1
HP:0010562 Keloids 1
HP:0010566 Hamartoma 1
HP:0010739 Osteopoikilosis 1
HP:0011868 Sciatica 1
HP:0012532 Chronic pain 1
HP:0012735 Cough 1
HP:0025247 Dermoid cyst 1
HP:0030411 Jejunal adenocarcinoma 1
HP:0030431 Osteochondroma 1
HP:0030834 Shoulder pain 1
HP:0031368 Intestinal perforation 1
HP:0031501 Pelvic mass 1
HP:0040276 Adenocarcinoma of the colon 1
HP:0100537 Fasciitis 1
HP:0100570 Carcinoid tumor 1
HP:0100614 Myositis 1
HP:0100621 Dysgerminoma 1
HP:0200008 Intestinal polyposis 1


Causative gene(s) retrieved from Orphanet

    Total: 2

Gene Symbol Gene Name Entrez Gene ID
CTNNB1 catenin beta 1 1499
APC APC regulator of WNT signaling pathway 324