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1 nal carcinoma, two chromophobe type, and one lipoma).
2 mour cell types, including fat-cell tumours (lipomas).
3  confidence rating of 4 or 5 as positive for lipoma.
4 well differentiated liposarcomas or atypical lipomas.
5 l segment rearranged in a subset of ordinary lipomas.
6 mosomal segment often rearranged in ordinary lipomas.
7 e and efficacious treatment of large colonic lipomas.
8 ce imaging (MRI) findings of rare pancreatic lipomas.
9 , macroscopic fat (<-30 HU) was present in 9 lipomas.
10  bile duct, stomach, oral cavity tumors, and lipomas.
11 gn ocular tumors, and central nervous system lipomas.
12 low accuracy in the diagnosis of soft-tissue lipomas.
13 ental ages, a cerebellar tumor, and multiple lipomas.
14 on, and have an abnormally high incidence of lipomas.
15 ntial role for HMG I-C in the development of lipomas.
16 nt to perturb adipogenesis and predispose to lipomas.
17 nign tumors of mesenchymal origin, including lipomas.
18 HMGI-C truncation in the generation of human lipomas.
19 ng multiple angiofibromas, collagenomas, and lipomas.
20 pathy (1 patient in each group), and gastric lipoma (0 and 1 patients, respectively).
21 tients had myelodysplastic lesions (19 filar lipoma, 14 syringomyelia, 10 intradural lipoma, eight de
22 astomas, 18 (6%) with fibromas, 12 (4%) with lipomas, 28 (9%) with other benign primary cardiac tumor
23  expression was detected in 7 of 11 ordinary lipomas (63.6%) with alterations at 12q14-15 and in one
24 Two patients presented with symptomatic cord lipomas after laparoscopic hernia repair.
25 ding frontonasal dysplasia, interhemispheric lipoma, agenesis of the corpus callosum, tibial hemimeli
26 tical tumors, angiofibroma, collagenoma, and lipoma, also occur in some patients.
27                                         Both lipoma and liposarcoma demonstrated thin septa and regio
28                        The incidence of cord lipoma and relationship to inguinal hernia were evaluate
29            Histologic examination yielded 25 lipomas and 14 nonlipomas.
30 39 well differentiated adipose neoplasms (19 lipomas and 20 ALTs) of known karyotype using polyclonal
31 ith histologically verified fatty tumors (35 lipomas and 25 well-differentiated liposarcomas) were re
32 motor dysfunction, subcutaneous and visceral lipomas and hemangiomas, and intestinal juvenile polypos
33 ibroma, 14 myxoma, 6 vascular, 4 teratoma, 3 lipoma, and 15 other.
34 to distinguish between liposarcoma subtypes, lipoma, and normal fat samples.
35 nal juvenile polyposis, developmental delay, lipomas, and pigmentation spots of the male genitalia.
36 er syndromes characterized by overgrowth and lipomas are part of the PTEN syndrome spectrum, we ascer
37                                              Lipomas are rare, small, homogenous and well-circumscrib
38                                   Pancreatic lipomas are reported to be rare but their prevalence is
39                     There were 32 (51%) cord lipomas associated with indirect hernias, 11 (17%) with
40 , progressive skeletal deformities, invasive lipomas, benign and malignant tumors, and deep venous th
41 ertained six individuals with overgrowth and lipomas but who did not meet the diagnostic criteria for
42  the level of confidence in the diagnosis of lipoma by using a five-point scale.
43                                     Epidural lipomas causing cord compression is documented in patien
44 mobility group proteins, is disrupted in 3/3 lipomas characterized by 12q14-q15 rearrangements.
45                                      Colonic lipomas (CL) are rare benign adipose tumours usually fou
46     Nonendocrine mesenchymal tumors, such as lipomas, collagenomas, and angiofibromas have also been
47 s tumors, epithelioid sarcomas, spindle cell lipomas, dermatofibrosarcoma protuberans, and myofibrobl
48  methemoglobin), 3.lipid-containing lesions (lipoma, dermoid cyst, implanted fatty materials, laminar
49 ilar lipoma, 14 syringomyelia, 10 intradural lipoma, eight dermal sinus, five diastematomyelia, five
50 lity and focal soft tissue tumors (fibromas, lipomas, etc).
51                Translocations of 12q13-15 in lipomas (fat cell tumors) disrupt HMGI-C and fuse its DN
52 n particular, increased abundance of fat and lipomas, features strikingly similar to those observed i
53 differentiated mesenchymal tumors, including lipomas, fibroadenomas of the breast, salivary gland ade
54 nal regulatory domains was not necessary for lipoma formation.
55          Chromosomal translocations in human lipomas frequently create fusion transcripts encoding hi
56 sion of other mesenchymal tumors (leiomyoma, lipoma, gastrointestinal stromal tumor, leiomyosarcoma,
57 feration of mesenchymal cells in leiomyomas, lipomas, hamartomas,and other diseases has been linked t
58 sferase 3) with stroke, and the LHFPL2 gene (lipoma high mobility group protein I-C fusion partner-li
59                                      Lhfpl2 (lipoma HMGIC fusion partner-like 2) encodes a tetra-tran
60 f hair cell stereocilia (TMHS, also known as lipoma HMGIC fusion partner-like 5, LHFPL5), both though
61 nding genes, nucleolar protein 4 (NOL4), and lipoma HMGIC fusion partner-like protein 4 (LHFPL4), whi
62                        We report a growth of lipoma in an unusual site in a 28-year-old female renal
63  "loop and let go" technique for large colon lipomas in a large case series.
64  study examined the prevalence of pancreatic lipomas in a sample of patients undergoing abdominal com
65 dministered, are implicated in the growth of lipomas in different anatomic locations including the ep
66 elopment of angiofibromas, collagenomas, and lipomas in patients with MEN1.
67 ontaining preferred translocation partner in lipoma), induced by constitutive activation of STAT5, bu
68 ic the mesenchymal submucosal tumors such as lipoma, leiomyoma, and gastrointestinal stromal tumors.
69        Paratesticular tumours can be benign (lipoma, leiomyoma, haemangioma) or malignant (rhabdomyos
70 69%), including those with either classic or lipoma-like histology, had rearrangements of the 8q12 PL
71 n that lipoblastomas can evolve into mature, lipoma-like, lesions.
72 s, range 8-24), there was one small residual lipoma (&lt;1 cm).
73                                          The lipomas measured between 4 and 12 mm.
74                                              Lipomas measured from 6 mm to 32 mm (average 12.8 mm) an
75                                            A lipoma of the cord is herniated fat that appears to orig
76     This is the first case of intramedullary lipoma of the spinal cord that may be related to steroid
77                                              Lipomas of the cord and round ligament occur with a sign
78                                  Sixty-three lipomas of the cord were identified for an incidence of
79 tivity was demonstrated in only two ordinary lipomas: one with 6p21 rearrangement and one with normal
80 al loci that may be perturbed during cardiac lipoma pathogenesis.
81  a family of proteins that also includes the lipoma preferred partner (LPP) and thyroid receptor-inte
82                                              Lipoma preferred partner (LPP) has been identified as a
83                                              Lipoma preferred partner (LPP) is a proline rich LIM dom
84  the adhesion plaque protein, zyxin, and the lipoma preferred partner (LPP).
85     Here, we found that CAFs upregulated the lipoma-preferred partner (LPP) gene in microvascular end
86 d receptor-interacting protein 6 (TRIP6) and lipoma-preferred partner (LPP), but not to zyxin itself.
87                          The echogenicity of lipomas ranged from hypoechoic to hyperechoic relative t
88 rare, karyotypically distinct group of human lipomas, rearrangements of 6p21-23 produce internal dele
89 ed with development of human tumors, such as lipomas, relatively few examples exist of germline mutat
90 igations of primary cardiac tumors (myxomas, lipomas, rhabdomyomas, and fibromas) have provided insig
91                                   Pancreatic lipomas seem to be quite a common finding and can be fou
92 x angiofibromas, three collagenomas, and one lipoma showed allelic deletion of the MEN1 gene.
93 pillary fibroelastomas (SMR 3.17, P=0.0003), lipomas (SMR 5.0, P=0.0003), other benign tumors (SMR 4.
94                Our patient had an intradural lipoma that had merged with the medulla of the spinal co
95 k features of BRR: macrocephaly and multiple lipomas, the latter of which occur in a minority of indi
96 ons consisted of six adenomatoid tumors, two lipomas, two epidermoid inclusion cysts, two cases of sa
97  differentiated mesenchymal tumors including lipomas, uterine leiomyomas, and pulmonary chondroid ham
98  that is rearranged in several solid tumors, lipomas, uterine leiomyomata, and liposarcomas.
99 he tendon sheath, epidermal inclusion cysts, lipomas, vascular lesions, peripheral-nerve tumours, ski
100                Additionally, the presence of lipomas was correlated with the presence of PTEN mutatio
101 peritoneal hernia repair, the anatomy of the lipomas was studied both at the time of surgery and agai
102                                   Forty-five lipomas were associated with hernias and were characteri
103                             Overall, 18 cord lipomas were found in groins without hernias, and these
104                                         Nine lipomas were found in women, seven presenting with groin
105               In 6 patients small pancreatic lipomas were found.
106                                          All lipomas were incidental findings unrelated to patients'
107                         Following diagnosis, lipomas were looped and ligated by endoloop.
108 y required for tumorigenesis, is bypassed in lipomas which express chimeric HMGI proteins.
109 88, average: 65.6 years), with 13 pancreatic lipomas, whose cases constituted the basis for 10 contra
110                      A significant number of lipomas will have prominent non-adipose areas and will d
111 ibed, consisting of looping and ligating the lipoma with a nylon snare.
112  ( > 25 kb) and is the site of disruption in lipomas with 12q14-q15 translocations.

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