Book contents
- Pearls and Pitfalls in Neoplastic Dermatopathology
- Pearls and Pitfalls in Neoplastic Dermatopathology
- Copyright page
- Dedication
- Contents
- Contributors
- Preface
- “It takes a village to raise a child”
- Chapter 1 Introduction
- Chapter 2 Keratinocytic tumors
- Chapter 3 Melanocytic tumors
- Chapter 4 Adnexal tumors
- Chapter 5 Hematolymphoid tumors
- Chapter 6 Fibrous and myofibroblastic tumors and reactive lesions
- Chapter 7 Neural tumors
- Chapter 8 Smooth and striated muscle tumors
- Chapter 9 Vascular and perivascular tumors, and tumor-like conditions
- Chapter 10 Adipocytic tumors
- Chapter 11 Bone and cartilage
- Chapter 12 Uncommon lineage-unrelated tumors
- Chapter 13 Cutaneous metastases
- Chapter 14 Medicolegal pitfalls in dermatopathology: perspectives from the USA and the UK
- Index
- References
Chapter 10 - Adipocytic tumors
Published online by Cambridge University Press: 05 July 2016
Book contents
- Pearls and Pitfalls in Neoplastic Dermatopathology
- Pearls and Pitfalls in Neoplastic Dermatopathology
- Copyright page
- Dedication
- Contents
- Contributors
- Preface
- “It takes a village to raise a child”
- Chapter 1 Introduction
- Chapter 2 Keratinocytic tumors
- Chapter 3 Melanocytic tumors
- Chapter 4 Adnexal tumors
- Chapter 5 Hematolymphoid tumors
- Chapter 6 Fibrous and myofibroblastic tumors and reactive lesions
- Chapter 7 Neural tumors
- Chapter 8 Smooth and striated muscle tumors
- Chapter 9 Vascular and perivascular tumors, and tumor-like conditions
- Chapter 10 Adipocytic tumors
- Chapter 11 Bone and cartilage
- Chapter 12 Uncommon lineage-unrelated tumors
- Chapter 13 Cutaneous metastases
- Chapter 14 Medicolegal pitfalls in dermatopathology: perspectives from the USA and the UK
- Index
- References
- Type
- Chapter
- Information
- Pearls and Pitfalls in Neoplastic Dermatopathology , pp. 417 - 429Publisher: Cambridge University PressPrint publication year: 2000
References
Primary Sources
Vantyghem, M.C., Balavoine, A.S., Douillard, C., et al. (2012). How to diagnose a lipodystrophy syndrome. Ann Endocrinol (Paris), 73, 170–89.CrossRefGoogle ScholarPubMed
Thway, K., Flora, R.S., and Fisher, C. (2012). Chondroid lipoma: an update and review. Ann Diagn Pathol, 16, 230–4.Google Scholar
Sheng, W., Lu, L., and Wang, J. (2013). Cellular angiolipoma: a clinicopathologic and immunohistochemical study of 12 cases. Am J Dermatopathol, 35, 220–5.CrossRefGoogle ScholarPubMed
Hameed, M. (2007). Pathology and genetics of adipocytic tumors. Cytogenet Genome Res, 118, 138–47.CrossRefGoogle ScholarPubMed
Wood, L., Fountaine, T.J., Rosamilia, L., et al. (2010). Cutaneous CD34+ spindle cell neoplasms: Histopathologic features distinguish spindle cell lipoma, solitary fibrous tumor, and dermatofibrosarcoma protuberans. Am J Dermatopathol, 32, 764–8.Google Scholar
Secondary Sources
Chung, E.B. and Enzinger, F.M. (1973). Benign lipoblastomatosis. An analysis of 35 cases. Cancer, 32, 482–92.3.0.CO;2-E>CrossRefGoogle ScholarPubMed
Mentzel, T., Calonje, E., and Fletcher, C.D. (1993). Lipoblastoma and lipoblastomatosis: a clinicopathologic study of 14 cases. Histopathology, 23, 527–33.Google Scholar
Collins, M.H. and Chatten, J. (1997). Lipoblastoma/lipoblastomatosis: a clinicopathologic study of 25 tumors. Am J Surg Pathol, 21, 1131–7.Google Scholar
Ende, L., Upton, J., Richkind, K.E., et al. (2008). Lipoblastoma. Appreciation of an expanded spectrum of disease through cytogenetic analysis. Arch Pathol Lab Med, 132, 1442–4.Google Scholar
Choi, J., Bouron Dal Soglio, D., Fortier, A., et al. (2014). Diagnostic utility of molecular and cytogenetic analysis in lipoblastoma: a study of two cases and review of the literature. Histopathology, 64, 731–40.Google Scholar
Furlong, M.A., Fanburg-Smith, J.C., and Miettinen, M. (2001). The morphologic spectrum of hibernoma: a clinicopathologic study of 170 cases. Am J Surg Pathol, 25, 809–14.CrossRefGoogle ScholarPubMed
Chirieac, L.R., Dekmezian, R.H., and Ayala, A.G. (2006). Characterization of the myxoid variant of hibernoma. Ann Diagn Pathol, 10, 104–6.Google Scholar
Moretti, V.M., Brooks, J.S., and Lackman, R.D. (2010). Spindle cell hibernoma: a clinicopathologic comparison of this new variant. Orthopedics, 33, 52–5.CrossRefGoogle ScholarPubMed
Gaffney, E.F., Hargreaves, H.K., Semple, E., et al. (1983). Hibernoma: distinctive light and electron microscopic features and relationship to brown adipose tissue. Hum Pathol, 14, 677–87.Google Scholar
Beals, C., Rogers, A., Wakely, P., et al. (2014). Hibernomas: a single-institution experience and review of literature. Med Oncol, 31, 1–7.CrossRefGoogle ScholarPubMed
Marshall-Taylor, C. and Fanburg-Smith, J.C. (2000). Hemosiderotic fibrohistiocytic lipomatous lesion: ten cases of a previously undescribed fatty lesion of the foot/ankle. Mod Pathol, 13, 1192–9.CrossRefGoogle ScholarPubMed
Browne, T.J. and Fletcher, C.D. (2006). Hemosiderotic fibrolipomatous tumor (so-called hemosiderotic fibrohistiocytic lipomatous tumor): analysis of 13 new cases in support of a distinctive entity. Histopathology, 48, 453–61.CrossRefGoogle Scholar
Kazakov, D.V., Sima, R., and Michal, M. (2005). Hemosiderotic fibrohistiocytic lipomatous lesion: clinical correlation with venous stasis. Virchows Arch, 447, 103–6.Google Scholar
Folpe, A.L. and Weiss, S.W. (2004). Pleomorphic hyalinizing angiectatic tumor: analysis of 41 cases supporting evolution from a distinctive precursor lesion. Am J Surg Pathol, 28, 1417–25.CrossRefGoogle ScholarPubMed
Luzar, B., Gasljevic, G., Juricic, V., et al. (2006). Hemosiderotic fibrohistiocytic lipomatous lesion: early pleomorphic hyalinizing angiectatic tumor? Pathol Int, 56, 283–6.Google Scholar
Antonescu, C.R., Zhang, L., Nielsen, G.P., et al. (2011). Consistent t (1;10) with rearrangements of TGFBR3 and MGEA5 in both myxoinflammatory fibroblastic sarcoma and hemosiderotic fibrolipomatous tumor. Genes Chromosomes Cancer, 50, 757–64.Google Scholar
Premalata, C.S., Rama Rao, C., Padma, M., et al. (2008). Myxoinflammatory fibroblastic sarcoma – report of a rare case at an unusual site with review of the literature. Int J Dermatol, 47, 68–71.Google Scholar
Choi, J., Bouron Dal Soglio, D., Fortier, A., et al. (2014). Diagnostic utility of molecular and cytogenetic analysis in lipoblastoma: a study of two cases and review of the literature. Histopathology, 64, 731–40.CrossRefGoogle ScholarPubMed
Coindre, J.M., Pédeutour, F., and Aurias, A. (2010). Well-differentiated and dedifferentiated liposarcomas. Virchows Arch, 456, 167–79.Google Scholar
Dei Tos, A.P., Mentzel, T., and Fletcher, C.D.M. (1998). Primary liposarcoma of the skin: a rare neoplasm with unusual high grade features. Am J Dermatopathol, 20, 332–8.Google Scholar
Dei Tos, A.P. (2000). Liposarcoma: new entities and evolving concepts. Ann Diagn Pathol, 4, 252–66.Google Scholar
Hornick, J.L., Bosenberg, M.W., Mentzel, T., et al. (2004). Pleomorphic liposarcoma. Clinicopathologic analysis of 57 cases. Am J Surg Pathol, 28, 1257–67.Google Scholar
Iwasa, Y. and Nakashima, Y. (2013). Dedifferentiated liposarcoma with lipoma-like well-differentiated liposarcoma: clinicopathologic study of 30 cases, with particular attention to the comingling pattern of well- and dedifferentiated components: a proposal for regrouping of the present subclassification of well-differentiated liposarcoma and dedifferentiated liposarcoma. Int J Surg Pathol, 21, 15–21.Google Scholar
Val-Bernal, J.F., González-Vela, M.C., and Cuevas, J. (2003). Primary purely intradermal pleomorphic liposarcoma. J Cutan Pathol, 30, 516–20.Google Scholar