Julie C Fanburg-Smith

Summary

Publications

  1. doi Genetics for the diagnosis and treatment of mesenchymal tumors
    Jerzy Lasota
    Department of Soft Tissue and Orthopedic Pathology, Armed Forces Institute of Pathology, Washington, DC 20306 6000, USA
    Semin Musculoskelet Radiol 11:215-30. 2007
  2. doi Soft tissue Rosai-Dorfman disease: 29 new lesions in 18 patients, with detection of polyomavirus antigen in 3 abdominal cases
    Wael Al-Daraji
    Orthopaedic and Soft Tissue Pathology Department, AFIP, Washington, DC 20306, USA
    Ann Diagn Pathol 14:309-16. 2010
  3. doi Reappraisal of mesenchymal chondrosarcoma: novel morphologic observations of the hyaline cartilage and endochondral ossification and beta-catenin, Sox9, and osteocalcin immunostaining of 22 cases
    Julie C Fanburg-Smith
    Department of Orthopedic and Soft Tissue Pathology, Armed Forces Institute of Pathology, Washington, DC 20306 6000, USA
    Hum Pathol 41:653-62. 2010
  4. doi Immunoprofile of mesenchymal chondrosarcoma: aberrant desmin and EMA expression, retention of INI1, and negative estrogen receptor in 22 female-predominant central nervous system and musculoskeletal cases
    Julie C Fanburg-Smith
    Department of Orthopaedic and Soft Tissue Pathology, Armed Forces Institute of Pathology, Washington, DC 20306 6000, USA
    Ann Diagn Pathol 14:8-14. 2010
  5. ncbi An update on plexiform fibrohistiocytic tumor and addition of 66 new cases from the Armed Forces Institute of Pathology, in honor of Franz M. Enzinger, MD
    Christopher Moosavi
    Department of Orthopaedic and Soft Tissue Pathology, Armed Forces Institute of Pathology, Washington, DC 20306 6000, USA
    Ann Diagn Pathol 11:313-9. 2007
  6. doi Sporadic cutaneous angiosarcomas generally lack hypoxia-inducible factor 1alpha: a histologic and immunohistochemical study of 45 cases
    Malak Abedalthagafi
    Department of Pathology, Georgetown University Medical Center, Washington, DC 20007, USA
    Ann Diagn Pathol 14:15-22. 2010
  7. pmc Quantitative analysis of activating alpha subunit of the G protein (Gsα) mutation by pyrosequencing in fibrous dysplasia and other bone lesions
    Qi Liang
    Division of Molecular Pathology, Department of Scientific Laboratories, Armed Forces Institute of Pathology, Washington, DC 20306, USA
    J Mol Diagn 13:137-42. 2011
  8. doi Focal myositis: a clinicopathologic study of 115 cases of an intramuscular mass-like reactive process
    Aaron Auerbach
    Department of Hematopathology, Armed Forces Institute of Pathology, Washington, DC, USA
    Am J Surg Pathol 33:1016-24. 2009
  9. ncbi Imaging of soft-tissue myxoma with emphasis on CT and MR and comparison of radiologic and pathologic findings
    Mark D Murphey
    Department of Radiologic Pathology, Armed Forces Inst of Pathology, 6825 16th St NW, Bldg 54, Rm M 127A, Washington, DC 20306, USA
    Radiology 225:215-24. 2002
  10. doi Orbital solitary fibrous tumor: encompassing terminology for hemangiopericytoma, giant cell angiofibroma, and fibrous histiocytoma of the orbit: reappraisal of 41 cases
    Emiko Furusato
    Department of Neuropathology and Ophthalmic Pathology, Armed Forces Institute of Pathology, Washington, DC 20306 6000, USA
    Hum Pathol 42:120-8. 2011

Collaborators

Detail Information

Publications19

  1. doi Genetics for the diagnosis and treatment of mesenchymal tumors
    Jerzy Lasota
    Department of Soft Tissue and Orthopedic Pathology, Armed Forces Institute of Pathology, Washington, DC 20306 6000, USA
    Semin Musculoskelet Radiol 11:215-30. 2007
    ..Cytogenetic and molecular genetic alterations identified in various mesenchymal tumors are often valuable for diagnosis, prognosis, and treatment strategies...
  2. doi Soft tissue Rosai-Dorfman disease: 29 new lesions in 18 patients, with detection of polyomavirus antigen in 3 abdominal cases
    Wael Al-Daraji
    Orthopaedic and Soft Tissue Pathology Department, AFIP, Washington, DC 20306, USA
    Ann Diagn Pathol 14:309-16. 2010
    ..The relationship of polyomavirus to the evolution of abdominal STRDD should be further explored...
  3. doi Reappraisal of mesenchymal chondrosarcoma: novel morphologic observations of the hyaline cartilage and endochondral ossification and beta-catenin, Sox9, and osteocalcin immunostaining of 22 cases
    Julie C Fanburg-Smith
    Department of Orthopedic and Soft Tissue Pathology, Armed Forces Institute of Pathology, Washington, DC 20306 6000, USA
    Hum Pathol 41:653-62. 2010
    ....
  4. doi Immunoprofile of mesenchymal chondrosarcoma: aberrant desmin and EMA expression, retention of INI1, and negative estrogen receptor in 22 female-predominant central nervous system and musculoskeletal cases
    Julie C Fanburg-Smith
    Department of Orthopaedic and Soft Tissue Pathology, Armed Forces Institute of Pathology, Washington, DC 20306 6000, USA
    Ann Diagn Pathol 14:8-14. 2010
    ..Retained INI1 separates these tumors from atypical teratoid tumor. Despite marked female predominance in our series, estrogen receptor is negative in mesenchymal chondrosarcoma...
  5. ncbi An update on plexiform fibrohistiocytic tumor and addition of 66 new cases from the Armed Forces Institute of Pathology, in honor of Franz M. Enzinger, MD
    Christopher Moosavi
    Department of Orthopaedic and Soft Tissue Pathology, Armed Forces Institute of Pathology, Washington, DC 20306 6000, USA
    Ann Diagn Pathol 11:313-9. 2007
    ..The relationship between PFHT and cellular neurothekeoma is also explored...
  6. doi Sporadic cutaneous angiosarcomas generally lack hypoxia-inducible factor 1alpha: a histologic and immunohistochemical study of 45 cases
    Malak Abedalthagafi
    Department of Pathology, Georgetown University Medical Center, Washington, DC 20007, USA
    Ann Diagn Pathol 14:15-22. 2010
    ..Cutaneous angiosarcoma generally lacks HIF-1alpha expression. Accordingly, the hypoxic response pathway is not thought to be a documentable common mechanism of angiogenesis in this entity...
  7. pmc Quantitative analysis of activating alpha subunit of the G protein (Gsα) mutation by pyrosequencing in fibrous dysplasia and other bone lesions
    Qi Liang
    Division of Molecular Pathology, Department of Scientific Laboratories, Armed Forces Institute of Pathology, Washington, DC 20306, USA
    J Mol Diagn 13:137-42. 2011
    ..Mutation analysis of the Gsα by pyrosequencing has significant potential for improving discrimination between FD and other BFOLs in problematic cases...
  8. doi Focal myositis: a clinicopathologic study of 115 cases of an intramuscular mass-like reactive process
    Aaron Auerbach
    Department of Hematopathology, Armed Forces Institute of Pathology, Washington, DC, USA
    Am J Surg Pathol 33:1016-24. 2009
    ..We wanted to discuss the detailed morphologic and immunophenotypic features of the largest reported group of focal myositis patients...
  9. ncbi Imaging of soft-tissue myxoma with emphasis on CT and MR and comparison of radiologic and pathologic findings
    Mark D Murphey
    Department of Radiologic Pathology, Armed Forces Inst of Pathology, 6825 16th St NW, Bldg 54, Rm M 127A, Washington, DC 20306, USA
    Radiology 225:215-24. 2002
    ..To determine the imaging characteristics of soft-tissue myxoma, with emphasis on computed tomographic (CT) and magnetic resonance (MR) imaging findings and pathologic comparison...
  10. doi Orbital solitary fibrous tumor: encompassing terminology for hemangiopericytoma, giant cell angiofibroma, and fibrous histiocytoma of the orbit: reappraisal of 41 cases
    Emiko Furusato
    Department of Neuropathology and Ophthalmic Pathology, Armed Forces Institute of Pathology, Washington, DC 20306 6000, USA
    Hum Pathol 42:120-8. 2011
    ....
  11. ncbi Melanoma markers in angiomyolipoma of the liver and kidney: a comparative study
    Hala R Makhlouf
    Department of Hepatic and Gastrointestinal Pathology, Armed Forces Institute of Pathology, Washington, DC 20306 6000, USA
    Arch Pathol Lab Med 126:49-55. 2002
    ..Melanoma markers, especially the new microphthalmia transcription factor (mitf), have not been previously compared in hepatic and renal angiomyolipomas...
  12. doi Primary gallbladder sarcoma: a clinicopathologic study of 15 cases, heterogeneous sarcomas with poor outcome, except pediatric botryoid rhabdomyosarcoma
    Wael I Al-Daraji
    Department of Soft Tissue and Orthopaedic Pathology, Armed Forces Institute of Pathology, Washington, DC 20306 6000, USA
    Am J Surg Pathol 33:826-34. 2009
    ..Primary gallbladder sarcoma (PGBS) is rare, with only 39 documented cases, with the predominant type being leiomyosarcoma...
  13. doi Fibroosseous [corrected] pseudotumor of the digit: a clinicopathologic study of 43 new cases
    Christopher A Moosavi
    Department of Soft Tissue and Orthopedic Pathology, Armed Forces Institute of Pathology, Washington, DC 20306 6000, USA
    Ann Diagn Pathol 12:21-8. 2008
    ..These lesions are the superficial and distal counterparts of MO. It is important to understand the morphology of FOPD to distinguish this type of lesion from other benign and malignant fibroosseous lesions...
  14. ncbi Imaging of synovial chondromatosis with radiologic-pathologic correlation
    Mark D Murphey
    Department of Radiologic Pathology, Armed Forces Institute of Pathology, Washington, DC 20306, USA
    Radiographics 27:1465-88. 2007
    ..Recognizing the appearances of primary synovial chondromatosis, which reflect their underlying pathologic characteristics, improves radiologic assessment and is important to optimize patient management...
  15. ncbi Primary pulmonary and mediastinal synovial sarcoma: a clinicopathologic study of 60 cases and comparison with five prior series
    Paul H Hartel
    Department of Pulmonary and Mediastinal Pathology, Armed Forces Institute of Pathology, Washington, DC 20306 6000, USA
    Mod Pathol 20:760-9. 2007
    ..Awareness of focal unusual histology can prevent misdiagnosis particularly in t(x;18)-negative tumors...
  16. ncbi Giant cell fibroblastoma: an update and addition of 86 new cases from the Armed Forces Institute of Pathology, in honor of Dr. Franz M. Enzinger
    Prakash Jha
    Department of Orthopaedic and Soft Tissue Pathology, Armed Forces Institute of Pathology, Washington DC 20306 6000, USA
    Ann Diagn Pathol 11:81-8. 2007
    ..Collectively, we now have even more convincing morphologic, immunophenotypic, and molecular evidence that GCF is on a spectrum with DFSP...
  17. ncbi Keratin expression in schwannoma; a study of 115 retroperitoneal and 22 peripheral schwannomas
    Julie C Fanburg-Smith
    Department of Soft Tissue Pathology, Armed Forces Institute of Pathology, Washington, DC 20306 6000, USA
    Mod Pathol 19:115-21. 2006
    ..However, focal expression of K1 and K7 cannot be ruled out. Keratin-positive schwannomas should not be confused with other keratin-positive tumors, such as sarcomatoid carcinoma, mesothelioma, and synovial sarcoma...
  18. ncbi Liposarcoma of the oral and salivary gland region: a clinicopathologic study of 18 cases with emphasis on specific sites, morphologic subtypes, and clinical outcome
    Julie C Fanburg-Smith
    Department of Soft Tissue, The Armed Forces Institute of Pathology, Washington, DC 20306, USA
    Mod Pathol 15:1020-31. 2002
    ..Complete local excision and careful patient follow-up, without adjuvant therapy, appears to be the best treatment for OSG liposarcoma...
  19. doi Congenital epulis of the newborn: 10 new cases of a rare oral tumor
    Esther L B Childers
    Department of Oral Diagnostic Services, Howard University College of Dentistry ELBC, Howard University College of Dentistry, Washington, DC 20059, USA
    Ann Diagn Pathol 15:157-61. 2011
    ..It may be separated from "granular cell tumor" by location, patient age, absence of cytoplasmic hyaline globules, solid growth pattern, pericytic proliferation, attenuated overlying epithelium, and negativity for S-100 protein...