• 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....

. 2016 ; 40 (5) : 599-607.

Jazyk angličtina Země Spojené státy americké

Typ dokumentu hodnotící studie, časopisecké články, práce podpořená grantem

Perzistentní odkaz   https://www.medvik.cz/link/bmc16027953

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

Najít záznam

Citační ukazatele

Nahrávání dat ...

    Možnosti archivace