Bone Marrow Diagnosis is an important source for all those that have to document bone marrow trephine biopsies. The textual content is succinct and concentrates at the middle info essential to make a correct analysis. each one diagnostic entity is observed by way of top of the range photographs which express usual and more odd examples of histological good points. This re-creation has been thoroughly revised and up-to-date all through and contains many new photos together with stipulations no longer illustrated within the first edition.
A easily written and well-illustrated textual content for the busy diagnostician
- Every part comprehensively revised by way of overseas staff of authors
- Over 900 top of the range color pictures to accompany every one diagnostic entity
- Coverage of cytology in sections in terms of myeloid dysplasias and acute leukemias
- Incorporates new WHO type of lymphomas and leukemias
- Author staff accelerated to incorporate specialists from Stanford collage, California
Chapter 1 advent (pages 1–4):
Chapter 2 the conventional Bone Marrow (pages 5–19):
Chapter three Human Immunodeficiency Virus an infection (pages 20–30):
Chapter four Anemias and Aplasias (pages 31–40):
Chapter five The Myelodysplastic Syndromes (pages 41–47):
Chapter 6 Myeloproliferative affliction (pages 48–69):
Chapter 7 Acute Leukemia (pages 70–89):
Chapter 8.1 Lymphomas (pages 90–101):
Chapter 8.2 Acute Lymphoblastic Leukemia and Lymphoblastic Lymphoma (pages 102–108):
Chapter 8.3 persistent Lymphocytic Leukemia (pages 109–115):
Chapter 8.4 Lymphoplasmacytic Lymphoma (Including Waldenstrom Macroglobulinemia) (pages 116–121):
Chapter 8.5 Mantle cellphone Lymphoma (pages 122–125):
Chapter 8.6 Follicular Lymphoma (pages 126–131):
Chapter 8.7 Marginal quarter B cellphone Lymphoma (Including Malt variety) (pages 132–134):
Chapter 8.8 bushy phone Leukemia (pages 135–141):
Chapter 8.9 a number of Myeloma (pages 142–152):
Chapter 8.10 Diffuse huge B cellphone Lymphoma (pages 153–158):
Chapter 8.11 Burkitt Lymphoma (pages 159–164):
Chapter 8.12 huge Granular Lymphocyte Leukemia (pages 165–167):
Chapter 8.13 Cutaneous T mobile Lymphoma (pages 168–169):
Chapter 8.14 Peripheral T cellphone Lymphomas, Unspecified (pages 170–172):
Chapter 8.15 Hepatosplenic T mobile Lymphoma (pages 173–174):
Chapter 8.16 Angioimmunoblastic T telephone Lymphoma (pages 175–177):
Chapter 8.17 grownup T mobilephone Lymphoma/Leukemia (pages 178–179):
Chapter 8.18 Anaplastic huge phone Lymphoma (pages 180–182):
Chapter nine Hodgkin Lymphoma (pages 183–189):
Chapter 10 Metastatic illness (pages 190–196):
Chapter eleven Miscellaneous (pages 197–208):
Chapter 12 Technical concerns (pages 209–213):
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Additional resources for Bone Marrow Diagnosis: An Illustrated Guide, Second Edition
Bone marrow biopsy in myelodysplastic syndromes; morphological characteristics and contribution to study of prognostic factors. Br J Haematol 1990; 75: 26–33. 11 Horny H-P, Wehrmann M, Schlicker HUH, et al. QBEND10 for the diagnosis of myelodysplastic syndromes in routinely processed bone marrow biopsy specimens. J Clin Pathol 1995; 48: 291–4. Bone Marrow Diagnosis: An illustrated guide, Second Edition David Brown, Kevin Gatter, Yasodha Natkunam, Roger Warnke Copyright © 2006 David Brown, Kevin Gatter, Yasodha Natkunam and Roger Warnke Chapter 6 Myeloproliferative disease Myeloproliferative disease (MPD) is a spectrum of clinical entities characterized by a neoplastic proliferation, believed to arise from a malignant transformation at the marrow stem cell level.
Eur J Haematol 1988; 41: 434–7. 47 6 Verhoef G, De Wolf-Peeters C, Kerim S, et al. Update on the prognostic implication of morphology, histology and karyotype in primary myelodysplastic syndromes. Hematol Pathol 1991; 5: 163–75. 7 Tricot G, De Wolf-Peeters C, Vlietinck R, et al. Bone marrow histology in myelodysplastic syndromes. Br J Haematol 1984; 58: 217–25. 8 Kitagawa M, Kamiyama R, Takemura T, et al. Bone marrow analysis of the myelodysplastic syndromes; histological and immunohistochemical features related to the evolution of overt leukemia.
14 Megakaryocytes clustering around dilated sinuses. Giemsa. Fig. 15 Fibrosis associated with abnormal megakaryocytes in ET. Giemsa. Diagnostic problems 1 Philadelphia chromosome positive cases. Less than 10% of patients with the clinical features of ET have a Philadelphia chromosome. In these patients the marrow histology is more akin to CML (Fig. 16). 5 The WHO classification has excluded these cases from the category of ET by definition although without any discussion of the topic. 6 Currently, the pathologist needs to be aware of these cases although they should be categorized as CML if following the current WHO classification.