-
Je něco špatně v tomto záznamu ?
Fumarate Hydratase-deficient Uterine Leiomyomas Occur in Both the Syndromic and Sporadic Settings
WJ. Harrison, J. Andrici, F. Maclean, R. Madadi-Ghahan, M. Farzin, L. Sioson, CW. Toon, A. Clarkson, N. Watson, J. Pickett, M. Field, A. Crook, K. Tucker, A. Goodwin, L. Anderson, B. Srinivasan, P. Grossmann, P. Martinek, O. Ondič, O. Hes, K....
Jazyk angličtina Země Spojené státy americké
Typ dokumentu hodnotící studie, časopisecké články, práce podpořená grantem
- MeSH
- čipová analýza tkání MeSH
- dospělí MeSH
- fenotyp MeSH
- fumarasa nedostatek genetika MeSH
- genetická predispozice k nemoci MeSH
- imunohistochemie MeSH
- leiomyomatóza enzymologie genetika patologie chirurgie MeSH
- lidé středního věku MeSH
- lidé MeSH
- mutace MeSH
- mutační analýza DNA MeSH
- nádorové biomarkery nedostatek genetika MeSH
- nádory dělohy enzymologie genetika patologie chirurgie MeSH
- nádory kůže enzymologie genetika patologie chirurgie MeSH
- prognóza MeSH
- syndrom MeSH
- Check Tag
- dospělí MeSH
- lidé středního věku MeSH
- lidé MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- hodnotící studie MeSH
- práce podpořená grantem MeSH
Hereditary leiomyomatosis and renal cell carcinoma (HLRCC) syndrome secondary to germline fumarate hydratase (FH) mutation presents with cutaneous and uterine leiomyomas, and a distinctive aggressive renal carcinoma. Identification of HLRCC patients presenting first with uterine leiomyomas may allow early intervention for renal carcinoma. We reviewed the morphology and immunohistochemical (IHC) findings in patients with uterine leiomyomas and confirmed or presumed HLRCC. IHC was also performed on a tissue microarray of unselected uterine leiomyomas and leiomyosarcomas. FH-deficient leiomyomas underwent Sanger and massively parallel sequencing on formalin-fixed paraffin-embedded tissue. All 5 patients with HLRCC had at least 1 FH-deficient leiomyoma: defined as completely negative FH staining with positive internal controls. One percent (12/1152) of unselected uterine leiomyomas but 0 of 88 leiomyosarcomas were FH deficient. FH-deficient leiomyoma patients were younger (42.7 vs. 48.8 y, P=0.024) and commonly demonstrated a distinctive hemangiopericytomatous vasculature. Other features reported to be associated with FH-deficient leiomyomas (hypercellularity, nuclear atypia, inclusion-like nucleoli, stromal edema) were inconstantly present. Somatic FH mutations were identified in 6 of 10 informative unselected FH-deficient leiomyomas. None of these mutations were found in the germline. We conclude that, while the great majority of patients with HLRCC will have FH-deficient leiomyomas, 1% of all uterine leiomyomas are FH deficient usually due to somatic inactivation. Although IHC screening for FH may have a role in confirming patients at high risk for hereditary disease before genetic testing, prospective identification of FH-deficient leiomyomas is of limited clinical benefit in screening unselected patients because of the relatively high incidence of somatic mutations.
Citace poskytuje Crossref.org
- 000
- 00000naa a2200000 a 4500
- 001
- bmc16027953
- 003
- CZ-PrNML
- 005
- 20161031105423.0
- 007
- ta
- 008
- 161005s2016 xxu f 000 0|eng||
- 009
- AR
- 024 7_
- $a 10.1097/PAS.0000000000000573 $2 doi
- 024 7_
- $a 10.1097/PAS.0000000000000573 $2 doi
- 035 __
- $a (PubMed)26574848
- 040 __
- $a ABA008 $b cze $d ABA008 $e AACR2
- 041 0_
- $a eng
- 044 __
- $a xxu
- 100 1_
- $a Harrison, Wesley J $u *University of Sydney ¶¶Cancer Genetics, Hormones and Cancer Group, Kolling Institute of Medical Research, Royal North Shore Hospital, Sydney †Cancer Diagnosis and Pathology Research Group, Kolling Institute of Medical Research §Department of Anatomical Pathology ¶Familial Cancer Clinic, Royal North Shore Hospital, St Leonards ‡Douglass Hanly Moir Pathology ∥Histopath Pathology, North Ryde #Department of Medical Oncology, Hereditary Cancer Clinic, Prince of Wales Hospital, Randwick **Department of Medical Oncology, Concord Hospital, Concord West ††Department of Tissue Pathology and Diagnostic Oncology, Royal Prince Alfred Hospital, Camperdown, NSW ‡‡Department of Anatomical Pathology, Mater Hospital, South Brisbane, Qld, Australia §§Šikl's Department of Pathology, University Hospital, Faculty of Medicine in Pilsen, Charles University in Prague, Prague, Czech Republic ∥∥Department of Pathology and Laboratory Medicine, Calgary Laboratory Services, University of Calgary, Calgary, AB, Canada.
- 245 10
- $a Fumarate Hydratase-deficient Uterine Leiomyomas Occur in Both the Syndromic and Sporadic Settings / $c WJ. Harrison, J. Andrici, F. Maclean, R. Madadi-Ghahan, M. Farzin, L. Sioson, CW. Toon, A. Clarkson, N. Watson, J. Pickett, M. Field, A. Crook, K. Tucker, A. Goodwin, L. Anderson, B. Srinivasan, P. Grossmann, P. Martinek, O. Ondič, O. Hes, K. Trpkov, RJ. Clifton-Bligh, T. Dwight, AJ. Gill,
- 520 9_
- $a Hereditary leiomyomatosis and renal cell carcinoma (HLRCC) syndrome secondary to germline fumarate hydratase (FH) mutation presents with cutaneous and uterine leiomyomas, and a distinctive aggressive renal carcinoma. Identification of HLRCC patients presenting first with uterine leiomyomas may allow early intervention for renal carcinoma. We reviewed the morphology and immunohistochemical (IHC) findings in patients with uterine leiomyomas and confirmed or presumed HLRCC. IHC was also performed on a tissue microarray of unselected uterine leiomyomas and leiomyosarcomas. FH-deficient leiomyomas underwent Sanger and massively parallel sequencing on formalin-fixed paraffin-embedded tissue. All 5 patients with HLRCC had at least 1 FH-deficient leiomyoma: defined as completely negative FH staining with positive internal controls. One percent (12/1152) of unselected uterine leiomyomas but 0 of 88 leiomyosarcomas were FH deficient. FH-deficient leiomyoma patients were younger (42.7 vs. 48.8 y, P=0.024) and commonly demonstrated a distinctive hemangiopericytomatous vasculature. Other features reported to be associated with FH-deficient leiomyomas (hypercellularity, nuclear atypia, inclusion-like nucleoli, stromal edema) were inconstantly present. Somatic FH mutations were identified in 6 of 10 informative unselected FH-deficient leiomyomas. None of these mutations were found in the germline. We conclude that, while the great majority of patients with HLRCC will have FH-deficient leiomyomas, 1% of all uterine leiomyomas are FH deficient usually due to somatic inactivation. Although IHC screening for FH may have a role in confirming patients at high risk for hereditary disease before genetic testing, prospective identification of FH-deficient leiomyomas is of limited clinical benefit in screening unselected patients because of the relatively high incidence of somatic mutations.
- 650 _2
- $a dospělí $7 D000328
- 650 _2
- $a nádorové biomarkery $x nedostatek $x genetika $7 D014408
- 650 _2
- $a mutační analýza DNA $7 D004252
- 650 _2
- $a ženské pohlaví $7 D005260
- 650 _2
- $a fumarasa $x nedostatek $x genetika $7 D005649
- 650 _2
- $a genetická predispozice k nemoci $7 D020022
- 650 _2
- $a lidé $7 D006801
- 650 _2
- $a imunohistochemie $7 D007150
- 650 _2
- $a leiomyomatóza $x enzymologie $x genetika $x patologie $x chirurgie $7 D018231
- 650 _2
- $a lidé středního věku $7 D008875
- 650 _2
- $a mutace $7 D009154
- 650 _2
- $a fenotyp $7 D010641
- 650 _2
- $a prognóza $7 D011379
- 650 _2
- $a nádory kůže $x enzymologie $x genetika $x patologie $x chirurgie $7 D012878
- 650 _2
- $a syndrom $7 D013577
- 650 _2
- $a čipová analýza tkání $7 D046888
- 650 _2
- $a nádory dělohy $x enzymologie $x genetika $x patologie $x chirurgie $7 D014594
- 655 _2
- $a hodnotící studie $7 D023362
- 655 _2
- $a časopisecké články $7 D016428
- 655 _2
- $a práce podpořená grantem $7 D013485
- 700 1_
- $a Andrici, Juliana $7 gn_A_00006643
- 700 1_
- $a Maclean, Fiona
- 700 1_
- $a Madadi-Ghahan, Raha
- 700 1_
- $a Farzin, Mahtab
- 700 1_
- $a Sioson, Loretta
- 700 1_
- $a Toon, Christopher W
- 700 1_
- $a Clarkson, Adele
- 700 1_
- $a Watson, Nicole
- 700 1_
- $a Pickett, Justine
- 700 1_
- $a Field, Michael
- 700 1_
- $a Crook, Ashley
- 700 1_
- $a Tucker, Katherine
- 700 1_
- $a Goodwin, Annabel
- 700 1_
- $a Anderson, Lyndal $7 gn_A_00006165
- 700 1_
- $a Srinivasan, Bhuvana
- 700 1_
- $a Grossmann, Petr
- 700 1_
- $a Martinek, Petr
- 700 1_
- $a Ondič, Ondrej
- 700 1_
- $a Hes, Ondřej
- 700 1_
- $a Trpkov, Kiril
- 700 1_
- $a Clifton-Bligh, Roderick J
- 700 1_
- $a Dwight, Trisha
- 700 1_
- $a Gill, Anthony J
- 773 0_
- $w MED00000304 $t The American journal of surgical pathology $x 1532-0979 $g Roč. 40, č. 5 (2016), s. 599-607
- 856 41
- $u https://pubmed.ncbi.nlm.nih.gov/26574848 $y Pubmed
- 910 __
- $a ABA008 $b sig $c sign $y a $z 0
- 990 __
- $a 20161005 $b ABA008
- 991 __
- $a 20161031105845 $b ABA008
- 999 __
- $a ok $b bmc $g 1166267 $s 952583
- BAS __
- $a 3
- BAS __
- $a PreBMC
- BMC __
- $a 2016 $b 40 $c 5 $d 599-607 $i 1532-0979 $m The American journal of surgical pathology $n Am J Surg Pathol $x MED00000304
- LZP __
- $a Pubmed-20161005