Pancreatoblastoma

Medical condition
Pancreatoblastoma
SpecialtyOncology
Relative incidences of various pancreatic neoplasms, with pancreatoblastoma annotated at center right.[1]

Pancreatoblastoma is a rare type of pancreatic cancer.[2] It occurs mainly in childhood[3] and has a relatively good prognosis.

Symptoms

Children with pancreatoblastoma rarely present with early-stage disease, instead, most present with locally advanced or metastatic disease. Common presenting symptoms include abdominal pain, emesis, and jaundice. A multidisciplinary approach including good clinical history, state of the art imaging, and careful pathology is often needed to establish the correct diagnosis.[4]

Pathology

Resected pancreatoblastomas can be quite large, ranging from 2 centimeters to 20 centimeters in size (1 to 8 inches). They are typically solid, soft masses. Under the microscope, at least two cell types are seen: cells with “acinar” differentiation, and cells forming small “squamoid” nests. The cells with acinar differentiation have some features of the normal acinar cell of the pancreas (the most common cell in the normal pancreas).[5]

Diagnosis

Treatment

If the tumor is operable, the first line of therapy should be surgical resection. Then, after surgical resection, adjuvant chemotherapy should be given, even in stage I disease. In patients with inoperable disease, chemotherapy alone should be given.[6] A multi-disciplinary approach to the treatment, including surgeons, oncologists, pathologists, radiologists, and radiation oncologists, is often the best approach to managing these patients.[4]

See also

  • Grayson Gilbert

References

  1. ^ Wang Y, Miller FH, Chen ZE, Merrick L, Mortele KJ, Hoff FL; et al. (2011). "Diffusion-weighted MR imaging of solid and cystic lesions of the pancreas". Radiographics. 31 (3): E47-64. doi:10.1148/rg.313105174. PMID 21721197.{{cite journal}}: CS1 maint: multiple names: authors list (link)
    Diagram by Mikael Häggström, M.D.
  2. ^ "Pancreatoblastoma". Archived from the original on 2004-06-02.
  3. ^ Naik VR, Jaafar H, Leow VM, Bhavaraju VM (March 2006). "Pancreatoblastoma: a rare tumour accidentally found" (PDF). Singapore Med J. 47 (3): 232–4. PMID 16518559.
  4. ^ a b "Pancreatic Cancer Multi-Disciplinary Clinic at Johns Hopkins University".
  5. ^ "Pancreatic Cancer Frequently Asked Questions".
  6. ^ http://www.orpha.net/data/patho/GB/uk-pancrea.pdf -

External links

Classification
D
  • ICD-O: M8971/3
  • MeSH: C537162 C537162, C537162
  • v
  • t
  • e
Digestive system neoplasia
GI tract
Upper
Esophagus
  • Squamous cell carcinoma
  • Adenocarcinoma
Stomach
Lower
Small intestine
Appendix
Colon/rectum
Anus
Upper and/or lower
Accessory
Liver
Biliary tract
Pancreas
Peritoneum
  • v
  • t
  • e
Not otherwise specified
Connective tissue neoplasm
Fibromatous
Fibroma/fibrosarcoma
Fibroma/fibromatosis
Histiocytoma/histiocytic sarcoma
Myxomatous
Fibroepithelial
Synovial-like
Lipomatous
Myomatous
General
Smooth muscle
Skeletal muscle
Complex mixed and stromal
Mesothelial