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Diagnostic Cytopathology Essentials E-Book

Diagnostic Cytopathology Essentials E-Book

Gabrijela Kocjan | Winifred Gray | Philippe Vielh | Tanya Levine | Ika Kardum-Skelin

(2013)

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Book Details

Abstract

Diagnostic Cytopathology Essentials is a succinct yet comprehensive guide to diagnosis in both non-gynecological and gynecological cytology. It provides quick answers to diagnostic problems in the cytological interpretation and recognition of a wide range of disease entities. With content derived from Diagnostic Cytopathology, 3rd Edition, the authoritative reference work by Winifred Gray and Gabrijela Kocjan, Diagnostic Cytopathology Essentials delivers the dependable guidance you need - in a user-friendly format that makes essential facts about any given condition easy to find and apply.

  • Consult this title on your favorite e-reader, conduct rapid searches, and adjust font sizes for optimal readability.
  • Efficiently review the key cytological features of a broad spectrum of disease entities with more than 1,300 images, consistently presented on opposing pages from the corresponding text summaries for ease of reference.
  • Find the answers you need quickly and easily using an at-a-glance bullet-point format and structure, with every section organized consistently to include Definition, Cytological Findings, and Differential Diagnosis.
  • Streamline decision making and avoid diagnostic pitfalls with the aid of Differential Diagnosis boxes.
  • Improve your diagnostic cytology skills by referencing representative Case Studies throughout.

 


Table of Contents

Section Title Page Action Price
Front cover cover
Diagnostic Cytopathology Essentials i
Copyright page iv
Table of Contents v
Foreword vii
List of contributors ix
Dedication xi
Acknowledgements xi
1 Introduction 1
2 Female genital tract 3
Contents 3
Normal anatomy of the gynaecological tract (Fig. 2.1) 3
Transformation zone (Figs 2.2–2.4) 4
Cytology of normal cells from the cervical transformation zone 6
Squamous cells (Figs 2.5–2.8) 6
Metaplastic cells (Figs 2.9–2.11) 6
Anucleate squames (Figs 2.12, 2.13) 6
Endocervical cells (Figs 2.14–2.19) 8
Endometrial cells (Figs 2.20–2.22) 8
Reserve cells (Figs 2.23, 2.24) 10
Inflammatory cells 10
Other inflammatory cells (Fig. 2.25) 10
Other findings in cervical samples 11
Spermatozoa (Fig. 2.26) 11
Infestations (Figs 2.27–2.29) 11
External/atmospheric contaminants (Figs 2.30–2.32) 11
Artefacts in processing (Figs 2.33, 2.34) 11
Pregnancy and post-partum (Fig. 2.35) 11
Post-menopausal changes (Figs 2.36–2.40) 11
Cytological findings in cervicitis/vaginitis 14
Non-specific changes (Figs 2.41–2.45) 14
Specific types (Figs 2.46–2.49) 14
Common cervical/vaginal microorganisms 16
Bacteria (Figs 2.50–2.52) 16
Protozoa (Figs 2.53–2.55) 16
Fungi (Figs 2.56–2.58) 16
Common viral infections 18
Human papillomavirus (HPV) 18
Microscopic appearances (Figs 2.59–2.61) 18
Diagnostic pitfalls 18
Herpes simplex virus infection (HSV) 19
Iatrogenic changes in cervical cytology 20
Hormonal therapy 20
Intrauterine devices (IUD) (Figs 2.63–2.65) 20
Diagnostic pitfalls 20
Iatrogenic changes – surgical intervention 21
Iatrogenic changes – radiation 22
Repair and regeneration in the cervix 23
Cervical sample adequacy 24
Conventional/direct smears 24
Liquid-based cytology samples (Figs 2.73, 2.74) 24
Reasons for inadequate samples 24
Cytology of CIN and cervical squamous cancer 25
Dyskaryosis and abnormal chromatin (Figs 2.75–2.80) 25
Other features of dyskaryotic cells 25
Grading of squamous dyskaryosis (Table 2.1) 25
Mild dyskaryosis/low-grade dyskaryosis (Figs 2.81–2.88) 28
Moderate and severe/high-grade dyskaryosis (Figs 2.89–2.105) 30
Invasive squamous cell carcinoma of the cervix 35
Diagnostic pitfalls for cytology of squamous cell carincoma (Figs 2.124–2.127) 37
Keratinising CIN III 37
Repair and regeneration 37
Borderline nuclear changes in cervical cytology (Figs 2.128–2.136) 38
Management of borderline nuclear changes 38
Glandular neoplasms in cervical cytology 40
Primary cervical adenocarcinoma (Figs 2.137–2.144 and Table 2.2) 40
Cytologic appearances of CGIN 40
Non-cervical adenocarcinoma (Figs 2.145–2.153) 42
Cytological appearances of endometrial adenocarcinoma 42
Diagnostic pitfalls of CGIN and adenocarcinoma (Figs 2.154–2.161 and Table 2.3) 44
Management of women with abnormal cervical cytology 46
Squamous dyskaryosis 46
Glandular dyskaryosis 46
Follow-up after treatment and HPV testing as ‘test of cure’ 46
Cytology of the vulva and vagina 47
VIN, VAIN and invasive malignancy (Figs 2.163–2.172) 47
Malignant melanoma (Figs 2.173–2.175) 49
Paget’s disease of the vulva (Figs 2.176, 2.177) 49
Uterine cytology 50
Cytology of normal directly sampled endometrium (Figs 2.178, 2.179) 50
Cytology of non-neoplastic conditions 50
Endometrial hyperplasia and/or malignancy (Figs 2.180–2.187) 51
Ovarian cytology 53
Non-neoplastic ovarian cysts (Figs 2.188–2.194) 53
Simple cysts – including serosal inclusion cysts, paraovarian cysts and regressing follicular cysts 55
Ovarian neoplasms (Figs 2.195, 2.196) 55
Serous cystadenoma 55
Mucinous cystadenoma 55
Borderline epithelial ovarian tumours (Fig. 2.197) 56
Malignant ovarian tumours (Figs 2.198–2.203) 56
Mature cystic teratoma (Figs 2.204, 2.205) 56
3 Respiratory 59
Contents 59
Introduction 59
Normal cytological findings 60
Reactive changes 62
Case Study 63
Reactive atypia due to drug toxicity 63
Common lung tumours 64
Diagnosis and management of lung tumours 64
Tumour spread 64
Lung cancer diagnosis by cytology (Figs 3.21–23) 64
Squamous cell carcinoma (SqCC) 66
Small cell carcinoma 69
Adenocarcinoma 71
Adenocarcinoma – lepidic predominant 73
Large cell carcinoma 75
Case Study (Fig 3.73) 76
Large cell tumour 76
Carcinoid tumours 77
Other lung tumours and metastases 79
Mesenchymal tumours and lymphomas 81
Pulmonary lymphomas, leukaemia 83
Mediastinal tumours 84
Mediastinal germ cell tumours (GCTs) 86
Lung infections 88
Bacterial infections 88
Chronic bacterial infections (Figs 3.120–3.125) 88
Bacterial infections: differential diagnosis 88
Pulmonary TB: cytological findings (Figs 3.120–3.125) 88
Viral infections 90
Fungal infections 92
Aspergillus spp.: clinical settings in lung 92
Pneumocystis jirovecii (previously P. carinii) 93
Other fungal infections (Figs 3.139–3.144) 94
Parasitic infections 95
Other pulmonary conditions 96
Chronic obstructive pulmonary disease (COPD) 96
Bronchiectasis (Fig. 3.151) 96
Allergic bronchopulmonary disease 97
Sarcoidosis (Figs 3.156, 3.157) 98
Diffuse parenchymal lung disease (Fig. 3.158) 99
Occupational lung diseases (Figs 3.159 and 3.160) 99
Iron pigment deposition (Fig. 3.161) 100
Lipoid pneumonitis (Fig 3.162) 100
Pulmonary alveolar proteinosis (Fig. 3.163) 101
Amyloidosis (Fig. 3.164) 101
Talc granuloma (Fig. 3.165) 101
4 Serous effusions 103
Contents 103
Introduction 103
Clinicopathological significance of serous effusions (Table 4.1) 104
Cytology of normal and reactive mesothelial cells 105
Mesothelial cells 105
Diagnostic pitfalls: non-specific reactive mesothelial cells (Figs 4.13–4.15) 107
Conditions causing non-specific effusions 107
‘Atypical’ mesothelial cells (Fig. 4.15) 107
Other benign findings in reactive effusions 108
Cytology of other cells/entities (Figs 4.18–4.23) 108
Benign reactive effusions with specific features 110
General diagnostic approach to malignant effusions 112
Metastatic carcinoma cells in serous effusions 113
Examples of metastatic carcinoma effusions from breast (Figs 4.42–4.44) 116
Examples of metastatic carcinoma effusions from lung (Figs 4.45–4.47) 116
Examples of metastatic effusions from female genital tract carcinomas (Figs 4.48–4.53) 117
Examples of metastatic carcinoma effusions: gastrointestinal tract (Figs 4.54–4.59) 118
Other metastatic carcinoma examples in effusions (Figs 4.60–4.63, Table 4.2) 119
Haematolymphoid malignancies in effusions (Figs 4.64–4.69) 120
Mesothelioma 123
Clinical details 123
Clues to cytological diagnosis (Tables 4.5, 4.6, p. 127) 124
Diagnostic approach: mesothelioma morphology (Tables 4.5, 4.6) 127
Diagnostic approach: immunocytochemistry (Fig. 4.86 and Tables 4.7, 4.8) 128
Immunomarker examples: malignant cell types (Figs 4.87–4.100) 130
5 Urine cytology 135
Contents 135
Introduction 135
Specimen types and appearances (Figs 5.1–5.9) 135
Instrumented samples (Figs 5.10–5.15) 137
Ileal conduit samples (Figs 5.16–5.18) 137
Malignancy in urine cytology (Figs 5.19–5.27) 139
Differential diagnosis in urothelial malignancy 143
Degenerative changes (Figs 5.37–5.39) 143
BK/human polyomavirus 143
Instrumentation effects (Figs 5.40–5.47) 144
Papillaroid groups 144
Lithiasis/calculus formation 144
Other reactive conditions 144
Other infections 144
6 Thyroid gland 147
Contents 147
Introduction (Figs 6.1–6.3) 147
Benign thyroid nodules 148
Types of goitre – diffuse enlargement of the thyroid 148
Thyroid cysts 150
Thyroglossal cyst 152
Thyroiditis 153
Subacute thyroiditis (de Quervain’s) (Figs 6.30–6.34) 154
Riedel’s thyroidtis (Riedel’s struma) (Figs 6.35–6.38) 155
Thyroid hyperplasia/hyperthyroidism 156
Follicular lesions 158
Thyroid neoplasms 160
Follicular and oncocytic (Hürthle cell) neoplasms 160
Papillary carcinoma 162
Papillary carcinoma: special types 164
Medullary carcinoma 166
Anaplastic carcinoma 168
FNA thyroid reporting categories and their management implications 170
7 Haemopoietic 173
Contents 173
Introduction 173
Fine needle aspiration of the lymph node 173
Bone marrow aspiration 174
The role of FNA in management of lymphadenopathy 174
Ancillary technologies and the tumour bank 175
Cytospin preparations 175
Flow cytometry 175
Molecular techniques 175
Normal lymph node 176
Non-specific lymph node hyperplasia (Fig. 7.4) 177
Reactive lymphadenopathy 178
Sinus histiocytosis – Rosai–Dorfmann disease (Fig. 7.5) 178
Granulomatous lymphadenopathy 178
Tuberculous lymphadenitis (Figs 7.6, 7.7) 178
Sarcoidosis (Fig. 7.8) 179
Kikuchi–Fujimoto disease – histiocytic necrotising lymphadenitis (Fig. 7.9) 179
Cat-scratch disease (Fig. 7.10) 179
Kimura’s disease (Fig. 7.11) 180
Castleman’s disease (giant or angiofollicular lymph node hyperplasia, lymphoid hamartoma) 181
Neoplastic lesions of lymph node 182
Lymphoid neoplasms 182
Precursor lymphoid neoplasms 183
Lymphoblastic leukaemia/lymphoma 183
Mature B-cell neoplasms 185
Chronic lymphocytic leukaemia/small lymphocytic lymphoma (CLL/SLL) 185
Marginal zone lymphoma (MZL) 187
Plasma cell myeloma and primary amyloidosis 189
Clinical variants of plasma cell myeloma 189
Mantle cell lymphoma 191
Follicular lymphoma (FL) 192
Diffuse large B-cell lymphoma (DLBCL) 193
Primary effusion lymphoma 195
Burkitt’s lymphoma/leukaemia 197
Mature T- and NK-cell neoplasms 198
Hepatosplenic T-cell lymphoma 198
Peripheral T-cell lymphoma, not otherwise specified (NOS) 199
Mycosis fungoides/Sézary syndrome 200
Angioimmunoblastic T-cell lymphoma (AITL) 201
Anaplastic large cell lymphoma (ALCL) 202
Hodgkin lymphoma 204
Immunodeficiency-associated lymphoproliferative disorders 205
Lymphoma associated with HIV infection 205
Post-transplant lymphoproliferative disorders (PTLD) 206
Lymph node metastases (Figs 7.69–7.77) 207
Myeloid neoplasms 209
Myeloproliferative neoplasms 210
Chronic myeloid leukaemia, BCR-ABL 1 positive (CML) 210
Polycythaemia vera (PV) 212
Primary myelofibrosis (PM) 213
Essential thrombocythaemia (ET) 214
Chronic eosinophilic leukaemia, not otherwise specified (CEL-NOS) 215
Mastocytosis 216
Myelodysplastic/myeloproliferative neoplasms (MDS/MPN) 217
Chronic myelomonocytic leukaemia (MDS/MPN-CMML) 217
Juvenile myelomonocytic leukaemia (MDS/MPN-JMML) 218
Myelodysplatic/myeloproliferative neoplasms, unclassifiable (MDS/MPN-U) 219
Myelodysplastic syndromes (MDS) 220
Refractory cytopenia with unilineage dysplasia (RCUD) 220
Refractory anaemia with ring sideroblasts (RARS) 221
Refractory cytopenia with multilineage dysplasia (RCMD) 222
Refractory anaemia with excess blasts (RAEB) 223
Myelodysplastic syndrome with isolated del(5q) 224
Myelodysplastic syndrome, unclassifiable (MDS-U) 225
Refractory cytopenia of childhood (RCC) 226
Acute myeloid leukaemia 227
Acute myeloid leukaemia with recurrent genetic abnormalities – acute myeloid leukaemia with t(8;21) 227
Acute myeloid leukaemia with recurrent genetic abnormalities – acute promyelocytic leukaemia (PML) 228
Acute myeloid leukaemia with recurrent genetic abnormalities – acute myeloid leukaemia with inv(16) or t(16;16) 229
Acute myeloid leukaemia with myelodysplastic-related changes 230
Acute myeloid leukaemia, not otherwise specified – acute myeloid leukaemia with minimal differentiation 231
Acute myeloid leukaemia, not otherwise specified – acute myeloid leukaemia without maturation 232
Acute myeloid leukaemia, not otherwise specified – acute myeloid leukaemia with maturation 233
Acute myeloid leukaemia, not otherwise specified – acute myelomonocytic leukaemia 234
Acute myeloid leukaemia, not otherwise specified – acute monoblastic and monocytic leukaemia 235
Acute myeloid leukaemia, not otherwise specified – acute erythroid leukaemia 236
Acute myeloid leukaemia, not otherwise specified – acute megakaryoblastic leukaemia 237
Acute leukaemia, not otherwise specified – acute basophilic leukaemia 238
Acute myeloid leukaemia, not otherwise specified – acute panmyelosis with myelofibrosis 239
Acute leukaemias of ambiguous lineage 240
Myeloid sarcoma 241
Histiocytic and dendritic cell neoplasms 242
Histiocytic sarcoma (HS) 242
Langerhans cell histiocytosis 243
Other rare dendritic cell tumours 244
Fibroblastic reticular cell tumour 244
8 Breast 245
Contents 245
The normal breast 245
FNA of palpable lesions: capillary technique (Fig. 8.6) 247
Galactocele and gynaecomastia 248
Galactocele 248
Gynaecomastia (Figs 8.9–8.11) 248
Inflammatory conditions 249
Fat necrosis 249
Periductal mastitis (Fig. 8.15) 250
Subareolar abscess (Figs 8.16, 8.17) 250
Granulomatous mastitis (Figs 8.18–8.21) 251
Abscess and acute mastitis (Fig. 8.22) 252
Sclerosing lymphocytic lobulitis (Fig. 8.23) 252
Benign breast changes (Figs 8.24–8.32) 253
Benign tumours and tumour-like lesions 255
Fibroadenoma (Figs 8.33–8.41) 255
Benign phyllodes tumour (Figs 8.42–8.46) 257
Tubular adenoma (Fig. 8.47) 258
Lactating adenoma and lactational changes in benign lesions (Figs 8.48, 8.49) 258
Mammary hamartoma 258
Other benign lesions (Figs 8.50–8.55) 259
Cytological findings and differential diagnosis of epidermoid cyst 259
Other benign lesions include: 259
Epithelial hyperplasia and tumour-like lesions 261
Epithelial hyperplasia without atypia (Figs 8.56–8.58) 261
Complex sclerosing and fibrocystic lesions (Figs 8.59–8.61) 262
Benign papillary lesions 262
Borderline epithelial lesions (Figs 8.62–8.67) 263
Columnar cell lesions (CCL) 263
Hyperplasia with atypia 263
Cellular (florid) papillary lesions 264
Lobular intraepithelial neoplasia 264
Common malignant breast epithelial tumours (Table 8.1, Box 8.1) 265
Ductal carcinoma (Figs 8.68–8.78) 267
Invasive lobular carcinoma (Figs 8.79–8.83) 269
Uncommon malignant breast epithelial tumours 270
Tubular carcinoma (Figs 8.84, 8.85) 270
Medullary carcinoma with lymphoid stroma (Fig. 8.86) 270
Mucinous (colloid) carcinoma (Fig. 8.87) 271
Neuroendocrine carcinoma (Figs 8.88, 8.89) 271
Papillary carcinoma (Figs 8.90, 8.91) 272
Apocrine carcinoma (Fig. 8.92) 272
Glycogen-rich (clear cell) carcinoma (Fig. 8.93) 273
Carcinoma with osteoclast-like stromal giant cells (Fig. 8.94) 273
Paget’s disease of the nipple (Fig. 8.95) 273
Metaplastic carcinoma/carcinosarcoma (Figs 8.96–8.98) 274
Malignant myoepithelioma 274
Primary sarcomas, lymphomas and metastatic tumours (Figs 8.99–8.107) 275
Reporting breast FNAs: the role of FNA in management 277
The role of the multidisciplinary team 277
The role of FNA in management of breast lesions (Fig. 8.108) 277
9 Salivary gland 279
Contents 279
Introduction (Figs 9.1–9.3) 279
Normal salivary gland (Figs 9.4–9.6) 280
Tumours of the salivary gland 281
Most common tumour types (WHO classification 2005*) 281
Benign tumours 281
Malignant tumours 281
Pleomorphic adenoma 282
Warthin’s tumour (adenolymphoma) 284
Benign salivary gland tumours: basal cell adenoma and myoepithelioma 286
Other benign salivary gland tumours 287
Malignant salivary gland neoplasms: acinic cell carcinoma (Figs 9.32–9.38) 288
Mucoepidermoid carcinoma (Figs 9.39–9.47) 290
Adenoid cystic carcinoma (Figs 9.48–9.53) 292
Squamous cells in salivary gland aspirates 294
Polymorphous low-grade adenocarcinoma (Figs 9.61–9.63) 296
Salivary duct carcinoma (Figs 9.64–9.66) 297
Rare types of salivary gland malignant tumours 298
Carcinoma ex-pleomorphic adenoma (Fig. 9.67) 298
Epimyoepithelial carcinoma (Fig. 9.69) 298
Other primary and metastatic malignant tumours (Figs 9.70–9.75) 298
Non-neoplastic conditions 300
Pathogenesis and clinical findings 300
Salivary gland cysts 302
Mucus cyst (mucocele) 302
Mucocele (Figs 9.86–9.88) 302
Lymphoepithelial and branchial cleft cyst 303
Myoepithelial sialadenitis (Figs 9.93–9.97) 304
Mucosa associated lymphoid tissue (MALT) lymphoma (Figs 9.96–9.101) 304
Hyaline globules and basaloid cells in salivary gland FNA 306
Oncocytic cells in salivary gland 307
Diagnostic approach to salivary gland FNA 308
10 Liver, biliary tree and pancreas 309
Chapter contents 309
Introduction 309
Liver 309
Normal cytology of the liver 310
Liver pigments and fatty change 311
Inflammatory and reactive conditions 312
Liver infections 312
Pyogenic abscess 312
Amoebic abscess 312
Actinomyces spp. abscess 312
Echinococcus spp. (Figs 10.9–10.11) 312
Granulomatous inflammation 312
Granulomata (non-infectious) 312
Lesions mimicking neoplasms 313
Bile duct hamartoma 313
Mesenchymal hamartoma 313
Inflammatory pseudotumour 313
Miscellaneous benign lesions 314
Benign neoplasms 315
Benign hepatic nodules 316
Dysplastic nodule 316
Focal nodular hyperplasia 316
Hepatocellular adenoma 316
Malignant neoplasms 318
Primary liver malignant neoplasms 318
Hepatocellular carcinoma 318
Variants of hepatocellular carcinoma 321
Fibrolamellar variant 321
Acinar cell variant 321
Clear cell variant 321
Hepatoblastoma 322
Cholangiocarcinoma 323
Angiosarcoma 324
Embryonal sarcoma 324
Metastatic liver tumours 325
Role of liver FNA in patient management 325
Gall bladder and extrahepatic bile ducts 326
Procedures for collecting cytological material from the biliary tree 326
Bile sampling 326
Brush or catheter samples 326
Liquid based cytology (LBC) 326
FNA samples 326
Normal cytology of bile ducts 327
Inflammatory and reactive processes of the biliary ducts 328
Parasitic infestation 328
Sclerosing cholangitis and stent placement (Fig. 10.57B) 328
Biliary Intraepithelial Neoplasia (BilIN) (previously dysplasia) 329
Neoplasms of the biliary tree 330
Biliary papillomatosis/intraductal papillary tumour 330
Cholangiocarcinoma 330
Special tumour types 331
Adenosquamous and squamous cell carcinoma (Fig. 10.65) 331
Villous adenoma and well-differentiated papillary carcinoma 331
Cystadenoma and cystadenocarcinoma 331
Pancreas 332
Normal cytology: pancreas 332
Pancreatitis 334
Acute pancreatitis 334
Chronic pancreatitis 334
Autoimmune pancreatitis (AIP) 335
Solid malignant neoplasms of the pancreas 336
Ductal adenocarcinoma 336
Variants of pancreatic ductal adenocarcinoma 338
Undifferentiated carcinoma 338
Adenosquamous carcinoma and acinar cell carcinoma 339
Solid pseudopapillary neoplasm of the pancreas (SPN) 340
Pancreatic endocrine neoplasm (PEN) 341
Poorly differentiated PEN (small cell carcinoma) (Fig. 10.99) 343
Pancreatic cysts 344
Non-neoplastic cysts of the pancreas 345
Pseudocyst 345
Lymphoepithelial cyst 345
Cystic neoplasms 346
Serous cystadenoma 346
Intraductal papillary mucinous neoplasm (IPMN) (Figs 10.104–10.109) 346
Mucinous cystic neoplasm (MCN) of the pancreas 349
The role of FNA in management of pancreatic lesions 350
11 Childhood tumours 351
Contents 351
Introduction 351
Role of the cytopathologist 351
Obtaining a cytological sample from a child 352
Main malignant small round cell tumours of childhood 352
Lymphoma 353
Neuroblastoma 354
Nephroblastoma (Figs 11.7, 11.8) 355
Rhabdomyosarcoma 357
Morphology and prognosis 357
Ewing’s (sarcoma) family of tumours (pPNET) 358
12 Miscellaneous 359
Contents 359
Cerebrospinal fluid 360
Clinical indications for CSF cytology 360
Preparation methods for CSF cytology 360
Inflammatory diseases (Fig. 12.4) 362
Bacterial infections (Fig. 12.4A–D) 362
Viral infections (Fig. 12.4E–G) 362
Fungal infections (Fig. 12.4H, I) 362
Other infectious causes 362
Unknown causes of inflammation 362
CSF in primary CNS tumours 363
CSF in secondary CNS tumours 364
CSF involvement in lymphomas and leukaemia 365
Skin 366
Sampling techniques 366
Skin infections 367
Pemphigus vulgaris, seborrhoeic keratosis, actinic keratosis, Bowen’s disease/carcinoma in situ 368
Seborrhoeic keratosis (Fig. 12.23) 368
Malignant tumours 369
Basal cell carcinoma 369
Squamous cell carcinoma, malignant melanoma 370
Other skin tumours 371
Soft tissue and musculoskeletal system 372
The role of FNA cytology in management of soft tissue and bone tumours 372
Technical procedures (Table 12.1) 372
FNA of soft tissue tumours 372
FNA of bone 372
Ancillary methods 372
Immunocytochemistry 372
Cytogenetics 372
Cytological findings in normal and reactive soft tissues 373
Soft tissue tumours 375
Benign soft tissue tumours (Figs 12.41–12.44) 375
Benign adipocytic tumours (Table 12.2) 375
Benign fibroblastic/myofibroblastic and fibrohistiocytic tumours 376
Nodular fasciitis 376
Proliferative myositis/fasciitis (Fig. 12.46) 376
Desmoid fibromatosis 376
Tumours of peripheral nerves 377
Miscellaeneous soft tissue tumours (Figs 12.51–12.54 and Table 12.3) 378
Malignant soft tissue tumours 379
Liposarcoma (Figs 12.55–12.57) 379
Malignant tumours of adipose tissue according to the WHO classification of soft tissue tumours 379
Rhabdomyosarcoma 381
Synovial sarcoma 382
Alveolar soft part sarcoma (Fig. 12.66) 382
Clear cell sarcoma (Fig. 12.67) 382
Skeletal tumours/lesions 383
Chondroma 383
Chondroblastoma 383
Chondrosarcoma 383
Osteogenic tumours 384
Osteoblastoma 384
Osteosarcoma 384
Bone: miscellaneous lesions 385
Langerhans cell histiocytosis (Fig. 12.73) 385
Ewing’s family of tumours (ES/PNET) 385
Bone: metastatic tumours and reporting of FNA in bone and soft tissue lesions 386
The cytological report 386
Synovial fluid 387
Basic approach to synovial fluid microscopy 387
The ‘wet prep’: crystal identification (Figs 12.75–12.78) 387
The ‘wet prep’: other particulate material (Fig. 12.79) 388
The cytocentrifuge preparation (Figs 12.80–12.82) 388
Management of synovial fluid cytology 389
13 Techniques 391
Contents 391
Routine procedures 392
Exfoliative cytology 392
Collection and transport of cytological material 392
General points 392
Fine needle aspiration cytology (FNAC) 394
Cytological preparations 394
Direct smear (Fig. 13.6) 394
Fluids (Fig. 13.7) 394
Cell block (Fig. 13.8) 394
Cell imprints (Fig. 13.9) 395
Liquid-based cytology (LBC) 395
Fixation 395
Most common pitfalls (Fig. 13.10) 395
Staining methods 396
Papanicolaou stain (Fig. 13.11) 396
May Grunwald Giemsa stain (Fig. 13.12) 396
Diagnostic pitfalls: PAP staining 397
Rapid staining method (Fig. 13.13) 397
The most commonly used histochemical stains on cytological preparations are 397
Immunocytochemistry 398
Introduction 398
Main applications of ICC 398
Sample preparation 398
Fixation 398
Fixatives 398
Antigen retrieval (AR) in ICC 398
Principles of ICC staining 399
Manually/automated 399
Direct/indirect methods (Fig. 13.15) 399
PAP method (Fig. 13.16) 399
ABC method (Fig. 13.17) 400
LSAB method (Fig. 13.18) 400
Polymeric methods (Fig. 13.19) 400
ICC staining 400
Internal quality control 401
Positive control (PC) 401
Negative control (NC) 401
External quality control 401
Pitfalls – weak reaction/no reaction 403
Pitfalls – background staining and unspecific bindage 403
Polymerase chain reaction 404
Introduction 404
Rationale 404
Sample types 404
Nucleic acid extraction 404
Techniques 405
Applications 405
Nucleic acid targets 405
Pitfalls 405
Clonality analysis to aid lymphoma diagnosis 406
Clonality analysis 406
Method of cell preparation in suspected lymphoma 406
PCR product analysis (Figs 13.39, 13.40) 406
Pitfalls 406
Chromosome translocation detection 407
Diagnosis of lymphomas 407
Diagnosis of sarcomas 407
Method: Lymphomas 407
Method: Sarcomas 407
Pitfalls 407
Mutation detection for therapy selection in lung cancer 408
Epidermal growth factor receptor (EGFR) 408
Selection of first-line therapy in non small cell lung carcinoma (NSCLC) 408
Pitfalls 408
PCR detection of infectious agents 409
Mycobacterial infection (Fig. 13.46) 409
Pitfalls in detection of infectious agents 409
Pneumocystis carinii (Fig. 13.47) 409
Future developments in molecular diagnostics 409
In situ hybridisation (ISH) (Figs 13.48, 13.49) 410
The principle 410
DNA probes 410
Fluorescence in situ hybridisation: protocol and laboratory equipment (Figs 13.50–13.52) 411
Types of preparation 411
FISH protocol flow chart 411
Fluorescence in situ hybridization in lymphomas: gene translocation (Figs 13.53–13.56) 412
Other translocations and genes detected by FISH in lymphomas 412
Fluorescence in situ hybridisation in solid tumours: detection of gene amplification (Figs 13.57–13.61) 413
Other solid tumours (different types), and the genes which are frequently amplified 413
Fluorescence in situ hybridisation in solid tumours: gene translocation (Figs 13.62–13.65) 414
Other mesenchymal solid tumours and genes involved in their pathogenesis detected by FISH 414
14 Self-assessment questions 415
Case 1 Routine cervical cytology sample from a 32-year-old woman 416
Subject Index 443
A 443
B 444
C 446
D 448
E 448
F 449
G 450
H 450
I 451
J 451
K 452
L 452
M 454
N 455
O 456
P 456
Q 458
R 458
S 458
T 460
U 461
V 462
W 462
X 462
Z 462