Σταδιοποίηση σε Ca Εξωκρινούς Μοίρας του Παγκρέατος

 

Ca Παγκρέατος – Εξωκρινής μοίρα

AJCC Stages

Stages

T

N

M

0

Tis

N0

M0

IA

T1

N0

M0

IB

T2

N0

M0

IIA

T3

N0

M0

IIB

T1

N1

M0

T2

N1

M0

T3

N1

M0

III

T4

Any N

M0

IV

Any T

Any N

M1

(T) Primary Tumor

TX

Primary tumor cannot be assessed

T0

No evidence of primary tumor

Tis

Carcinoma in situ*

T1

Tumor limited to the pancreas, ≤ 2 cm in greatest dimension

T2

Tumor limited to the pancreas, > 2 cm in greatest dimension

T3

Tumor extends beyond the pancreas but without involvement of the celiac axis or the superior mesenteric artery

T4

Tumor involves the celiac axis or the superior mesenteric artery (unresectable primary tumor)

*This also includes the "PanInIII" classification.

(N) Regional Lymph Nodes

NX

Regional lymph nodes cannot be assessed

N0

No regional lymph node metastasis

N1

Regional lymph node metastasis

(M) Distant Metastasis

M0

No distant metastasis

M1

Distant metastasis

Χαρακτηριστικά Επέκτασης

Local invasion

  • Vascular invasion
    • Celiac trunk
    • Superior mesenteric artery (SMA)
    • Common and proper hepatic artery
    • Gastroduodenal artery (GDA)
    • Splenic artery
    • Portal vein
    • Superior mesenteric vein (SMV)
    • Splenic vein
  • Primary tumor in pancreatic head &/or uncinate
    • Duodenum
    • Stomach
    • Inferior vena cava
    • Aorta
    • Right renal artery
  • Primary tumor in pancreatic body &/or tail
    • Transverse colon and mesocolon
    • Stomach
    • Left renal vein
    • Left adrenal gland
    • Superior pole of left kidney
    • Spleen
    • Splenic flexure of colon
    • Inferior vena cava
    • Aorta

Lymphatic spread

  • Pancreatic head and uncinate tumors
    • Anterior and superior pancreatic head
      • Drain along anterior superior pancreaticoduodenal vessels to pyloric and celiac axis nodes
  • Posterior and superior pancreatic head
    • Drain along posterior superior pancreaticoduodenal vessels to pyloric and celiac axis nodes or along common bile duct to portal vein and to hepatic hilar nodes
  • Inferior pancreatic head and uncinate
    • Drain along inferior pancreaticoduodenal vessels to superior mesenteric and paraaortic nodes
  • Pancreatic body and tail tumors
    • Drain either along splenic artery to celiac axis nodes or splenic hilar nodes

Perineural/perivascular spread

  • Pathways similar to lymphatic spread of tumor
  • 80% of pancreatic carcinomas demonstrate perineural invasion on pathology

Hematogenous spread

  • Occurs late in disease, but common for patients to have hematogenous metastases at time of presentation
  • Hepatic metastases are common
    • Pancreas drained by portal venous structures
    • Hepatic sinusoids lack basement membrane and are relatively porous, which is thought to allow metastases to permeate into space of Disse
  • Distant hematogenous metastases are less common and generally only seen in advanced disease (lung, pleura, adrenal glands, brain, bone, other)

Peritoneal spread

  • Common location of metastatic disease

Κατηγοριοποίηση (Ιστολογικοί Τύποι)

Ductal origin (> 95%)

  • Ductal adenocarcinoma (> 85%)
  • Cystic mucinous carcinoma
  • Noncystic mucinous carcinoma (colloid Ca)
    • Associated with more protracted course
  • Undifferentiated carcinoma
    • Sarcomatoid (spindle cell)
    • Anaplastic giant cell
    • Carcinosarcoma
    • Undifferentiated carcinoma with osteoclast-like giant cells
  • Adenosquamous carcinoma
  • Intraductal papillary mucinous carcinoma
  • Signet ring cell carcinoma
  • Serous cystadenocarcinoma (very rare)
  • Medullary carcinoma (very rare)

Acinar origin (1-2%)

  • Acinar cell carcinoma

Mixed origin

  • Mixed ductal-endocrine carcinoma (rare)
    • Behaves similar to ductal carcinoma
  • Mixed ductal-acinar carcinoma (rare)
    • Behaves similar to ductal carcinoma
  • Mixed acinar-endocrine carcinoma
    • Behaves similar to acinar carcinoma
  • Pancreatoblastoma
    • Typically includes all 3 cell types (endocrine, ductal, acinar) but composed of cells of acinar origin
    • Typically in children (peak age: 4 years) with small 2nd peak in 4th decade of life

Supportive element origin

  • Squamous cell carcinoma (very rare)

Unknown origin

  • Solid pseudopapillary carcinoma

Borderline, indolent, or premalignant neoplasms
(up to 2% of exocrine pancreatic Ca arise from these)

  • Intraductal papillary mucinous neoplasm    (IPMN)
  • Pancreatic intraepithelial neoplasia III (PanInIII)
  • Mucinous cystadenoma
  • Intraductal oncocytic papillary neoplasm (rare)
  • Solid pseudopapillary tumor

According to 2010 AJCC staging guidelines, pancreatic exocrine and endocrine tumors now utilize same staging system, which was previously reserved for exocrine pancreatic carcinoma

 

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