Oncocytic Melanoma: A Study of a Rare Entity

被引:0
作者
Donner, Ludvik R. [1 ]
Maximo, Valdemar [2 ,3 ,4 ]
机构
[1] Baylor Scott & White Hlth, Temple, TX USA
[2] Univ Porto, Inst Res & Innovat Hlth, Inst Invest & Inovacao Saude I3S, Porto, Portugal
[3] Univ Porto, IPATIMUP Inst Mol Pathol & Immunol, Porto, Portugal
[4] Univ Porto, Fac Med, Dept Pathol, Porto, Portugal
关键词
oncocytic melanoma; mtDNA; MALIGNANT-MELANOMA; MITOCHONDRIAL-DNA; UNUSUAL VARIANTS; MUTATIONS; PHENOTYPE; FEATURES;
D O I
10.1097/DAD.0000000000001183
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
The authors report the second case of oncocytic melanoma, one of the rarest known melanoma variants. The diagnosis was established by Fontana stain positivity, expression of S100 protein as well as gp100/HMB45, and demonstration of numerous mitochondria by ultrastructure. Because it is known that some oncocytic tumors of the thyroid gland and kidney contain point mutations and common deletions of mitochondrial DNA, the complete mitochondrial DNA of the reported oncocytic melanoma was also studied. It was normal except for 2 private separate point mutations, predicted to be not pathogenic, which do not seem to play any role in the tumor phenotype.
引用
收藏
页码:854 / 856
页数:3
相关论文
共 12 条
  • [1] Abbott JJ, 2004, ARCH PATHOL LAB MED, V128, P686
  • [2] Unusual variants of malignant melanoma
    Barnhill, Raymond L.
    Gupta, Kapil
    [J]. CLINICS IN DERMATOLOGY, 2009, 27 (06) : 564 - 587
  • [3] Primary malignant melanoma with rhabdoid features: A histologic and immunocytochemical study of three cases
    Borek, BT
    McKee, PH
    Freeman, JA
    Maguire, B
    Brander, WL
    Calonje, E
    [J]. AMERICAN JOURNAL OF DERMATOPATHOLOGY, 1998, 20 (02) : 123 - 127
  • [4] Clonal expansion of mutated mitochondrial DNA is associated with tumor formation and complex I deficiency in the benign renal oncocytoma
    Gasparre, Giuseppe
    Hervouet, Eric
    de Laplanche, Elodie
    Demont, Jocelyne
    Pennisi, Lucia Fiammetta
    Colombel, Marc
    Mege-Lechevallier, Florence
    Scoazec, Jean-Yves
    Bonora, Elena
    Smeets, Roel
    Smeitink, Jan
    Lazar, Vladimir
    Lespinasse, James
    Giraud, Sophie
    Godinot, Catherine
    Romeo, Giovanni
    Simonnet, Helene
    [J]. HUMAN MOLECULAR GENETICS, 2008, 17 (07) : 986 - 995
  • [5] Disruptive mitochondrial DNA mutations in complex I subunits are markers of oncocytic phenotype in thyroid tumors
    Gasparre, Giuseppe
    Porcelli, Anna Maria
    Bonora, Elena
    Pennisi, Lucia Fiammetta
    Toller, Matteo
    Iommarini, Luisa
    Ghelli, Anna
    Moretti, Massimo
    Betts, Christine M.
    Martinelli, Giuseppe Nicola
    Ceroni, Alberto Rinaldi
    Curcio, Francesco
    Carelli, Valerio
    Rugolo, Michela
    Tallini, Giovanni
    Romeo, Giovanni
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2007, 104 (21) : 9001 - 9006
  • [6] Metastatic rhabdoid melanoma: report of a case with a comparative review of the literature
    Gavino, Alde Carlo P.
    Gillies, Elizabeth M.
    [J]. JOURNAL OF CUTANEOUS PATHOLOGY, 2008, 35 (03) : 337 - 342
  • [7] Oncocytic metaplasia occurring in melanoma
    Jih, DM
    Morgan, MB
    Bass, J
    Tuthill, R
    Somach, SC
    [J]. SEMINARS IN CUTANEOUS MEDICINE AND SURGERY, 2004, 23 (01) : 73 - 79
  • [8] Primary Cutaneous Signet-Ring Cell Melanoma With Pseudoglandular Features, Spindle Cells and Oncocytoid Changes
    Kacerovska, Denisa
    Sokol, Ladislav
    Michal, Michal
    Kazakov, Dmitry V.
    [J]. AMERICAN JOURNAL OF DERMATOPATHOLOGY, 2009, 31 (01) : 81 - 83
  • [9] Major genomic mitochondrial lineages delineate early human expansions
    Maca-Meyer, Nicole
    Gonzalez, Ana M.
    Larruga, Jose M.
    Flores, Carlos
    Cabrera, Vicente M.
    [J]. BMC GENETICS, 2001, 2 (1)
  • [10] Unusual variants of malignant melanoma
    Magro, CM
    Crowson, AN
    Mihm, MC
    [J]. MODERN PATHOLOGY, 2006, 19 : S41 - S70