Invasive breast carcinoma - IARC

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MPNST, see Malignant peripheral nerve sheath tumour MRE11, 341 MSH2, 53, 118, 132, 337, 342, 358-361 MSH6, 53, 337, 342, 358-361 MSI, 53, 359-361 MSI-H, 360, 361 Mucin producing carcinoma, 30 Mucinous adenocarcinoma, 124, 206, 212, 221, 224, 272, 273, 297, 300 Mucinous borderline tumour, 124-126, 128, 145, 193 Mucinous borderline tumour, intestinal type, 125 Mucinous carcinoid, 171, 173, 195 Mucinous carcinoma, 30, 31, 34, 35, 57, 80, 124-126, 128, 195, 206, 226, 339 Mucinous cystadenocarc i n o f i b roma, 124 Mucinous cystadenocarcinoma, 30-32, 145 Mucinous cystadenoma, 124-127, 129, 143, 156, 175, 209, 212 Mucinous cystic tumours with mural nodules, 127 Mucinous tumour of borderline malignancy, endocervical-like, 126 Mucinous tumour of borderline malignancy, intestinal type, 125 Mucinous tumour of low malignant potential, endocervical-like, 126 Mucinous tumour of low malignant potential, intestinal type, 125 Mucocoele-like lesion, 31 Mucoepidermoid carcinoma, 39, 277 Mucoid carcinoma, 30, 42 Mucosal/acral lentiginous melanoma, 331 Muir-Torre syndrome, 132 MUL, 51 Müllerian papilloma, 276, 300 Multicystic mesothelioma, 197, 198 Multilocular peritoneal inclusion cyst, 198 Multinodular goitre, 356 Multinucleated giant cells, 92, 99, 207 Multiple facial trichilemmomas, 356 Multiple hamartoma syndrome, 355 MutL homologue 1, 359 MutL homologue 3, 359 MutS homologue 2, 359 MutS homologue 6, 359 Myc, 250, 266 Myoepithelial carcinoma, 40, 86, 88, 92 Myoepitheliosis, 86 Myofibroblastoma, 91 Myoglobin, 246, 302 Myoid hamartoma, 103 Myxoid leiomyoma, 236, 241 Myxoid leiomyosarcoma, 238 Myxoma, 182, 187, 244 N NCOA3 (AIB1), 51, 343, 350 Neuroblastoma, 51, 174, 334 Neuroendocrine carcinoma, 30, 43, 184, 279, 333 N e u roendocrine tumours, 32, 144, 277, 279 Neurofibroma, 94, 329, 330 Neuron-specific enolase, 200, 255 Nevoid basal cell carcinoma syndrome, 151 NFKB / NF-kappaB, 352, 362 Nipple adenoma, 81, 104 Nipple discharge, 68, 74, 76, 77, 85, 92, 97, 101, 112 Nipple duct adenoma, 104 Nodular adenosis with apocrine metaplasia, 85 Nodular hidradenoma, 324, 325 Nodular melanoma, 331 Nodular theca-lutein hyperplasia of pregnancy, 188 Non-encapsulated sclerosing lesion, 83 Non-gestational choriocarcinoma, 163, 167, 168 Non-keratinizing, squamous cell carcinoma, 266, 267, 316, 317 Non-medullary thyroid cancer, 355 Nuclear grooves, 86, 147 O O6-Methylguanine DNA ethyltransferase (O6MGMT) 353 Ollier disease, 149 Oncocytic carcinoma, 43 Ordinary intraductal hyperplasia, 65 Osteosarcoma, 40, 97, 98, 101, 175, 188, 244, 246, 282 Ovarian tumour of probable wolffian origin, 186 Ovarian wolffian tumour, 182, 186 P p14ARF, 353 p16/CDKN2a/p16INK4, 270, 353 p21, 250, 341, 348 p27, 58 p63, 86 p73, 362 Paget disease, 23, 35, 41, 63, 68, 105, 112, 174, 319, 321, 322, 324, 332, 352 Paget disease of the nipple, 35, 41, 105 Pagetoid spread, 332, 333 Paneth cell, 45, 125-127, 272, 276 Papillary adenoma, 104 Papillary carcinoma, non-invasive, 78 Papillary ductal carcinoma in situ, 79 Papillary hidradenoma, 321, 323 Papillary intraductal carcinoma, 32, 34, 79 Papillary squamous cell carcinoma, 267 Papilloma, 76-79, 119, 209, 296 Papillomatosis, 76, 104, 271, 296 Papillomatosis of the nipple, 104 Paraganglioma, 182, 187, 255, 283 Parasitic leiomyoma, 239 Parathyroid hormone-related protein, 138 Partial hydatidiform mole, 254 PAT1, 51 PDGFRL, 52 Peau d’orange, 48 PEComa, 243 Peptide YY, 172 Periductal stromal sarcoma, 100, 102 Peripheral papilloma, 76-78, 83 Peripheral primitive neuroectodermal tumour, 244, 255, 309, 334 Peritoneal mesothelioma, 185,197, 199 Peritoneal mucinous carcinomatosis, 128 Peritoneal tumours, 197 Perivascular epithelioid cell tumour, 243 Peutz-Jeghers syndrome, 156-158, 208, 273 Phaeochromocytoma, 187 Phosphoinositol-3-kinase, 357 Phyllodes tumour, 96, 97, 99-101, 103, 247, 352 Pigmented progonoma, 175 PIVKA-II (protein induced by vitamin K absence), 184 Placental alkaline phosphatase, 196 430 Subject Index
Placental site nodule, 211, 252, 254 Placental site trophoblastic tumour, 210, 250-252 Placental-like alkaline phosphatase (PLAP) 164, 168, 191, 252 Plasma cell granuloma, 93 Plasmacytoma, 192 Pleomorphic adenoma, 41, 85, 86, 88, 307, 324 Pleomorphic carcinoma, 21, 41 Pleomorphic lobular carcinoma, 24, 25 Plexiform leiomyoma, 241 PMS1, 53, 360 PMS2, 53, 359, 360 PNET, see Primitive neuroectodermal tumour P o l y e m b ryoma, 163, 167, 168 Polypoid adenofibroma, 209 Polyvesicular vitelline tumour, 165 Postmeiotic segregation 2, 359 Postoperative spindle cell nodule, 244, 281, 283, 305, 326 Post-radiotherapy angiosarcoma, 96 Potter syndrome, 149 Primary peritoneal borderline tumour, 197, 202 Primary peritoneal carcinoma, 197, 201 Primitive neuro e c t o d e rmal tumour, 171,174, 309, 310 Proliferating trichilemmal tumour, 325 Prophylactic bilateral mastectomy, 345 Prophylactic bilateral salpingooophorectomy, 345 Proteus syndrome, 357 Protocadherin 9, 112 Proximal-type epithelioid sarcoma, 326 pS2, 72 Psammocarcinoma, 201, 202 Psammoma bodies, 68, 119, 122, 198, 202, 210, 214, 224, 225, 255, 274, 276 Pseudoangiomatous hyperplasia, 103 Pseudoangiomatous stromal hyperplasia, 90 Pseudocarcinomatous hyperplasia, 209 Pseudomyxoma ovarii, 129 Pseudomyxoma peritonei, 126, 128, 129, 208 PTEN, 131, 132, 145, 230-232, 318, 354-357, 359 R Rad50, 341 RAD51, 341-343, 348-351 Radial scar, 26, 27, 39, 60, 78, 81-83 Radial sclerosing lesion, 83 RASSF1A (Ras association domain family 1A gene), 52 RB1CC1 (RB1-inducible Coiled-Coil 1), 52 Reichert membrane, 165 Reifenstein syndrome, 112 Reinke crystals, 154, 158, 160, 161, 176, 177 Renin, 157, 207 Rete cyst, 124 Rete ovarii adenocarcinoma, 180 Rete ovarii adenoma, 180 Retiform Sertoli-Leydig cell tumour, 156 Retiform wolffian adenocarcinoma, 212 Retiform wolffian adenoma, 212 Retiform wolffian tumour, 186 Retinal anlage tumour, 171, 175 Revised Amsterdam Criteria, 358 Rhabdoid tumour, 244 Rhabdomyoma, 244, 282, 305, 330 Rhabdomyosarcoma, 40, 97, 101, 109, 135, 155, 175, 188, 244, 302, 309, 311, 326 RING domain, 342 Rokitansky protuberance, 163, 171 RPS6KB1, 51 S Salpingitis isthmica nodosa, 210 Sarcoma botryoides, 155, 248, 280, 281, 283, 297, 302, 303, 305, 309, 326 Sarcoma family syndrome of Li and Fraumeni, 351 Schiller-Duval bodies, 165 Schwannoma, 94, 283, 304, 330 Scleroelastotic scar, 83 Sclerosing adenosis, 27, 39, 60, 61, 78, 81-83, 86, 98, 99, 104 Sclerosing papillary lesion, 39, 83 Sclerosing papilloma, 77, 85, 104 S c l e rosing papillomatosis, 104 S c l e rosing peritonitis, 149, 150 Sclerosing stromal tumour, 149, 152 SCTAT, see Sex cord tumor with annular tubules Sebaceous adenoma, 171, 175 Sebaceous carcinoma, 37, 46, 47, 171, 175, 324 Sebocrine cell, 47 Seborrheic keratosis, 321 Secretory carcinoma, 42 Secretory variant, endometrioid adenocarcinoma, 130, 221, 223 Seminoma, 163, 164, 176, 177 Serotonin, 143, 173, 272, 279 Serous adenocarcinoma, 119, 141, 201, 206, 212, 221, 224-226, 272, 274, 339 Serous adenofibroma, 119 Serous borderline adenofibroma, 122 Serous borderline tumour, 119, 120, 121, 127, 144, 202, 209 Serous borderline tumour with microinvasion, 120 Serous cystadenoma, 119, 124, 209, 212 Serous papillary cystadenoma, 119 Serous psammocarcinoma, 119, 120 Serous surface borderline tumour, 122 Serous tumour of borderline malignancy, 120, 121 Serous tumour of borderline malignancy with microinvasion, 120 Serous tumour of low malignant potential with microinvasion, 120 Serous tumour of low malignant potential,, 121 Sertoli cell tumour, 153, 156-159, 179, 196, 213 Sertoli cell tumour, annular tubular variant, 158 Sertoli-Leydig cell tumour, 131, 153, 157, 159, 172, 180, 188, 196, 213 Sertoli-Leydig tumour with heterologous elements, 155 Sex cord tumour with annular tubules, 157-159, 179, 273 Sex hormone-binding globulin, 16 Signet ring cell carcinoma, 30, 32, 42 Signet-ring cell, 138, 272, 273 Signet-ring cell adenocarcinoma, 193, 273 Signet-ring stromal tumour, 153 Simple atypical hyperplasia of the endometrium, 229 Simple hyperplasia of the endometrium, 229 Site specific early onset breast cancer syndrome, 346 SIX1 homeobox gene, 72 Subject Index 431
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Previous volumes in this series Kle
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World Health Organization Classific
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Published by IARC Press, Internatio
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CHAPTER 1 Tumours of the Breast Can
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TNM classification of carcinomas of
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Invasive breast carcinoma I.O. Elli
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Rapid growth and greater adult heig
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tives, administrative and clerical
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Grade 1 - well differentiated: 3-5
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ent and this is occasionally extens
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Most melanotic tumours of the breas
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A Fig. 1.22 A Classic invasive lobu
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yet others at 90% {97,2147}. For pr
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Fig. 1.27 Medullary carcinoma. The
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myoepithelial cells in fibro a d e
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A Fig. 1.33 Neuroendocrine carcinom
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Macroscopy Fisher et al. reported t
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Fig. 1.39 Apocrine carcinoma. Note
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cells contain intracytoplasmic lume
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A Fig. 1.50 Carcinosarcoma. A Two a
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A B C Fig. 1.75 Lobular neoplasia.
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Intraductal proliferative lesions F
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A B absence of either microcalcific
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Fig. 1.83 Atypical ductal hyperplas
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A B Fig. 1.88 Large excision biopsy
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unusual variants as well. Using thi
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esemble those identified in invasiv
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A B Fig. 1.97 Microinvasive carcino
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A Papilloma may be subject to morph
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A B C Fig. 1.103 Papillary intraduc
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colour measuring from 0.5 to 12 cm.
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Immunoprofile The cases studied by
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Glycogen-rich, clear cell carcinoma
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Differential diagnosis There may be
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quality metaphase spreads from an i
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Fig. 1.67 Lobular carcinoma of brea
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detectable distant metastasis displ
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detected at a late stage as small t
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Extent of ductal carcinoma in situ
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Benign epithelial proliferations G.
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Fig. 1.112 Microglandular adenosis.
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A Apocrine adenoma ICD-O code 8401/
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A B Fig. 1.128 Adenomyoepithelioma,
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Mesenchymal tumours M. Drijkoningen
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1113,1275}. There is a complex patt
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A B Fig. 1.137 A Lipoma. Intraparen
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Fig. 1.141 Angiosarcoma after breas
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A Fig. 1.144 Mammary osteosarcoma.
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Fibroepithelial tumours J.P. Belloc
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aged women (average age of presenta
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lished data suggests a 21% rate of
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A Fig. 1.157 Syringomatous adenoma
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Malignant lymphoma and metastatic t
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used. Inflammatory conditions in th
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male population both in the USA and
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CHAPTER 2 Tumours of the Ovary and
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Polyembryoma 9072/3 Non-gestational
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Surface epithelial-stromal tumours
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A Fig. 2.04 A Serous borderline tum
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A Fig. 2.06 Serous borderline tumou
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A Fig. 2.10 Invasive peritoneal imp
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Fig. 2.15 Mucinous carcinoma with i
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Fig. 2.20 Mucinous endocervical-lik
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A Fig. 2.28 Mucinous cystic tumour
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early secretory endometrium {2605}.
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IV, 6% {2233}. Patients with grade
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A Fig. 2.37 A This polypoid intracy
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Fig. 2.40 Endometrioid cyst with at
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1 tumours are extremely rare. Almos
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Fig. 2.50 Borderline Brenner tumour
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express thrombomodulin and have bee
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serous and transitional cell carcin
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is yellow to tan with a variable ad
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Genetic susceptibility JGCTs may pr
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Clinical features F i b romas may b
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distinguishes this tumour from the
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A Fig. 2.77 A Retiform Sertoli-Leyd
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Mean ages of 21 and 38 years and me
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Tumours unassociated with PJS form
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mal origin without crystals of Rein
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Germ cell tumours F. Nogales A. Tal
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cases, anisokaryosis has no prognos
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ation may coexist in the same neopl
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Table 2.06 Grading of ovarian immat
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A B Fig. 2.102 A Mature cystic tera
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Diagnostic procedures Elevated urin
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associated with mature teratomas sh
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atives intimately admixed. The germ
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Fig. 2.113 Mixed germ cell-sex cord
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A Fig. 2.116 A Adenomatous hyperpla
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Fig. 2.117 Small cell carcinoma, hy
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Clinical features Adenoid cystic-li
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Histopathology This epithelial tumo
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sis. Corpus luteum of pregnancy has
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Lymphomas and leukaemias L.M. Roth
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Secondary tumours of the ovary J. P
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Occasionally, the colonic adenocarc
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Peritoneal tumours S.C. Mok J.O. Sc
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A B Fig. 2.140 Cystic adenomatoid m
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whelmingly poor {1038,1547,2310}. H
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CHAPTER 3 Tumours of the Fallopian
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TNM and FIGO classification of carc
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Endometrioid adenocarcinoma Endomet
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Two examples of adenofibroma of bor
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A Fig. 3.11 Adenomatoid tumour. A T
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Clinical features Patients range in
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Fig. 3.16 Uterus-like mass. The cys
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CHAPTER 4 Tumours of the Uterine Co
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TNM and FIGO classification of non-
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Epithelial tumours and related lesi
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endometrioid adenocarcinoma fro m a
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fers from the prototypical type I e
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the ovary and bladder. Unlike prima
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schema {1535,2602}. Although this c
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Table 4.03 Altered gene function in
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Mesenchymal tumours and related les
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areas are limited to less than 30%
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A B C Fig. 4.30 Leiomyosarcoma. A T
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e used sparingly and is reserved fo
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A B Fig. 4.38 Leiomyoma with perino
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cytological atypia, tumour cell nec
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Mixed epithelial and mesenchymal tu
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Prognosis and predictive factors Th
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tumours may superficially invade th
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A Fig. 4.46 A Gestational choriocar
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A Fig. 4.49 A Classic complete hyda
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Sex cord-like, neuroectodermal and
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Secondary tumours of the uterine co
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WHO histological classification of
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Epithelial tumours M. Wells J.M. Ne
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Fig. 5.04 Mechanisms of human papil
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Fig. 5.08 Keratinizing squamous cel
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in their Asian population {2957}. I
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have a strong association with high
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e red by squamous epithelium {380}.
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endometrioid adenocarcinoma of the
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metrial epithelium. In some cases t
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with distinct cell borders and a gr
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Mesenchymal tumours M.L. Carcangiu
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{781}, liposarcoma {2840,3016}, ost
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Mixed epithelial and mesenchymal tu
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Fig. 5.44 Wilms tumour. The tumour
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A Fig. 5.47 Implant of endometrial
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CHAPTER 6 Tumours of the Vagina Alt
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Epithelial tumours E.S. Andersen A.
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Aetiology The fact that both VAIN a
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Fig. 6.10 Fibroepithelial polyp.A m
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er of mitoses varies but is usually
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ICD-O codes Adenosquamous carcinoma
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A C Fig. 6.17 Sarcoma botryoides. A
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1-11 cm. They may arise anywhere in
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elsewhere in the female genital tra
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A Fig. 6.24 Yolk sac tumour. A The
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g rowing in sheets. Some may have s
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WHO histological classification of
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Epithelial tumours E.J. Wilkinson M
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even with additional sectioning, it
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type) is a highly diff e rentiated
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Clinical features Bartholin gland c
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glandular elements surrounded by fi
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Mesenchymal tumours R.L. Kempson M.
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Table 7.03 Differential diagnosis o
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Prognosis and predictive factors A
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Table 7.04 Clark levels of cutaneou
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A Fig. 7.23 Vulvar peripheral primi
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Familial aggregation of cancers of
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BRCA1 syndrome Definition Inherited
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dispose individuals to the developm
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Fig. 8.05 To assess whether wild-ty
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Fig. 8.07 Factors that modify risk
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BRCA2 syndrome R. Eeles S. Piver S.
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tubal or ovarian carcinomas. Howeve
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in typical nuclear foci that may re
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Breast tumours Frequency Breast can
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Fig. 8.14 Codon distribution of som
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Breast tumours Age distribution and
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Hereditary non-polyposis colon canc
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essary in the evaluation of the pat
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Age distribution and penetrance Mos
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Contributors Dr Vera M. ABELER** De
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Dr Carlo LA VECCHIA Laboratory of E
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Dr Manuel TEIXEIRA Department of Ge
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02.100 Dr. A. Ostor 02.101 Dr. F.A.
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52. Akhtar M, Robinson C, Ashraf Al
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180. Bapat K, Brustein S (1989). Ut
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307. Bolis GB, Maccio T (2000). Cle
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436. Chang J, Sharpe JC, A'Hern RP,
Page 378 and 379: 562. Costa MJ, Ames PF, Walls J, Ro
Page 380 and 381: 689. Di Domenico A, Stangl F, Benni
Page 382 and 383: 820. Falck J, Petrini JH, Williams
Page 384 and 385: 943. Gad A, Azzopardi JG (1975). Lo
Page 386 and 387: 1067. Grimes MM (1992). Cystosarcom
Page 388 and 389: 1197. Herod JJ, Shafi MI, Rollason
Page 390 and 391: 1323. Jacques SM, Qureshi F, Ramire
Page 392 and 393: 1449. Khalifa MA, Mannel RS, Harawa
Page 394 and 395: 1564. Lagios MD (1977). Multicentri
Page 396 and 397: 1687. Loman N, Johannsson O, Kristo
Page 398 and 399: 1807. McCluggage G, McBride H, Maxw
Page 400 and 401: 1937. Mukai M, Torikata C, Iri H (1
Page 402 and 403: 2056. Norris HJ, Taylor HB (1967).
Page 404 and 405: 2180. Park JS, Jones RW, McLean MR,
Page 406 and 407: 2304. Puls LE, Hamous J, Morrow MS,
Page 408 and 409: 2 4 3 4 . Rosen PP, Groshen S, Saig
Page 410 and 411: 2559. Schlesinger C, Silverberg SG
Page 412 and 413: 2686. Silverberg SG (1999). Protoco
Page 414 and 415: 2806. Stutz JA, Evans AJ, Pinder S,
Page 416 and 417: 2942. Tornos C, Silva EG, Ordonez N
Page 418 and 419: 3061. Wargotz ES, Norris HJ (1990).
Page 420 and 421: 3189. Yoshioka T, Tanaka T (2000).
Page 422 and 423: References 425
Page 424 and 425: Biphasic teratomas, 168 BLM, 341, 3
Page 426 and 427: G GADD45, 343, 353 GCDFP-15, 25, 33
Page 430: Small cell / oat cell carcinoma, 32
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