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472 Part IV Stomach and Duodenum
exposure of the celiac, splenic, and hepatic arteries and their associated nodal beds. When a D2 node dissection is to be performed, these nodal beds are cleared of lymphatic tissue. Ideally, dissection of these nodes is delayed until the duode­num has been divided in order to facilitate exposure.
e gastroduodenal junction is palpated and evaluated for distal tumor involvement. If the area appears free of malig­nancy, the duodenum is divided 1–2 cm distal to the pylorus (Fig. 22-6). If tumor is palpable at the pylorus or proximal duodenal bulb, the duodenum is divided 1–2 cm distal to that point to obtain a microscopically negative resection margin. In this situation, however, care must be taken not to injure the retroduodenal portion of the common bile duct, the minor papilla, or the ampulla of Vater. e gastroduode­nal artery serves as a useful landmark as it passes behind the duodenal bulb. e retroduodenal common bile duct usually lies within 1 cm to the right of this vessel. We generally com­plete the division of the duodenum with a GIA stapler. Oth­ers prefer to transect the duodenum between bowel clamps and close the duodenal stump with a running 3-0 absorb­able monolament suture such as PDS. ere are no data to support the superiority of one method over the other. Some surgeons invaginate the duodenal staple/suture line with interrupted sutures in a standard Lembert fashion (Fig. 22-7).
If a D2 node dissection is performed, division of the duodenum provides improved exposure to the nodal bear­ing tissue adjacent to the hepatic, celiac, and splenic arteries located along the superior border of the pancreas. is tis­sue should be dissected and cleared from the region of the gastroduodenal artery to the basin adjacent to the proximal splenic artery. Care must be taken not to injure the pancreatic parenchyma or the celiac plexus.
Dissection of the lesser omentum is completed along thelesser curvature of the stomach from the inferior edge of the
A
FIGURE 22-6 e duodenum is divided 1–2 cm distal to the pylorus.
B
FIGURE 22-7 A. and B. e duodenal staple/suture line is invaginated
with interrupted Lembert sutures.
hepatoduodenal ligament to the right crus of the diaphragm. e retroperitoneal incision created along the lateral border of the second portion of the duodenum is extended superiorly to the conuence with the hepatoduodenal ligament at the inferior aspect of the foramen of Winslow. Next, the left lobe of the liver is retracted superiorly and to the right to expose the region of the diaphragmatic hiatus. e hepatogastric liga­ment is then incised from the diaphragmatic crus anterior to the gastroesophageal junction and along the hepatic border to the level of the porta hepatis at its conuence with the hepa­toduodenal ligament (Fig. 22-8). e incision is then carried
Chapter 22 Gastric Adenocarcinoma and Other Gastric Neoplasms (Except Gastrointestinal Stromal Tumors) 473
FIGURE 22-8 e hepatogastric ligament is incised from the dia-
phragmatic crus anterior to the gastroesophageal junction and along the hepatic border from the porta hepatis to the hepatoduodenal ligament.
FIGURE 22-9 e left gastric artery and vein are exposed and ligated.
e retroperitoneal dissection is carried to the left and inferiorly to join the retroperitoneal resection margin along the superior border of the pancreas.
inferiorly along the left border of the left hepatic artery to just above the junction with the duodenum, then medically to join with the retroperitoneal incision created previously. e hepa­toduodenal ligament is then incised superiorly at the level of the cystic duct, and then reected medially, exposing the struc­tures of the porta hepatis inferiorly. e superior and inferior resection margins of the hepatoduodenal ligament are carried posteriorly behind the portal vein. e right gastric artery and vein are identied, ligated, and transected. e hepatoduode­nal ligament that had been freed circumferentially from the porta hepatis can now be taken along with the nodal bearing connective tissue medial to the portal triad. e retroperitoneal dissection is then continued to the right of the aorta superiorly to the median arcuate ligament. e left gastric artery and vein are then exposed and ligated at their origins. If a D2 dissection is to be completed, dissection and clearance of the nodal bear­ing tissue around the left gastric artery should be performed at this point. e retroperitoneal dissection is then carried to the left and inferiorly to join the retroperitoneal resection margin along the superior border of the pancreas (Fig. 22-9).
e point of proximal gastric resection must be determined based on the location of the lesion. is requires resection of the entire lesion with a minimum 5-cm margin free of cancer. For a distal gastrectomy, the proximal resection plane is cre­ated from approximately 2 cm distal to the esophagogastric junction along the lesser curvature to a point along the greater curvature that will allow for a 5-cm resection margin. Divi­sion of the remaining greater omentum is performed to the level of the greater curvature resection point either by dividing between clamps and suture ligating the short gastric vessels or with an appropriate surgical energy source. Care should be exercised to avoid injury to the short gastric vessels located in the unresected greater omentum. With the proximal resection
line delineated, the stomach is transected either between clamps or with a surgical stapler (Fig. 22-10). e en bloc specimen should be marked to orient the pathologist to the appropriate margins and sent for frozen pathological analy­sis to ensure an adequate resection margin free of cancer has been obtained. Failure to obtain a cancer-free resection margin necessitates one or more attempted proximal gastric resections until appropriate margins are obtained if anatomically feasible.
Once the resection is complete, the decision as to which
reconstructive technique will be used must be made. We
FIGURE 22-10 With the proximal resection line delineated, the
stomach is transected either between clamps or with a surgical stapler.
474 Part IV Stomach and Duodenum
generally perform a Billroth II reconstruction. For details on reconstructive options and surgical techniques, please review the section on operative reconstruction options below.
Total Gastrectomy
e surgical approach for a proximal gastric lesion is very similar to that outlined previously for a distal gastric lesion. e only major variation is completion of the proximal dis­section at the gastroesophageal junction and diaphragmatic crura with en bloc removal of the gastric pericardial and paraesophageal lymph nodes (Fig. 22-11). e dissection of the omentum along the greater curvature must also be completed, taking care to divide the remaining short gastric vessels close to the spleen. Once the preceding dissection is completed, the proximal transaction margin is identied on the esophagus, just proximal to the gastroesophageal junc­tion. Esophageal division can be completed with an intesti­nal stapling device or an angled bowel clamp can be placed proximal to the planned transaction margin using a scalpel to divide the esophagus (Fig. 22-12). As with the distal gas­trectomy, frozen-section analysis of the proximal margin must be completed in order to ensure a curative resection. If a cancer-free margin cannot be obtained, the surgeon must determine whether the patient is a candidate for a curative esophagogastrectomy. Once the en bloc resection is com­plete and frozen-section pathological analysis has conrmed adequate operative margins, the intestinal reconstruction must be completed through the use of a Roux-en-Y esoph­agojejunostomy. e surgical approach to this reconstructive method is described in detail in the following text.
FIGURE 22-12 Esophageal division is completed with an intestinal
stapling device or an angled bowel clamp.
GASTROINTESTINAL RECONSTRUCTIVE TECHNIQUES
When determining the appropriate reconstructive method to restore intestinal continuity after gastric resection, it is important to choose a technique that will minimize long­term postoperative nutritional deciencies. common of these complications include marked weight loss
77–79
and dumping syndrome.
Some authors have asserted that this is best accomplished by restoring gastroduodenal integ­rity through construction of a jejunal interposition graft after
80–82
total or subtotal gastrectomy.
Although numerous case reports and case series have been published on various jeju­nal interposition techniques, there is currently no convincing evidence to support their use or a consensus on a standardized or optimal technique. Given the lack of adequate scientic evidence to support the merits of jejunal interposition grafts, we do not currently recommend their use. What does seem clear from published studies is that the most important con­cepts of reconstruction are to choose a technique that restores gastrointestinal continuity while reducing the incidence of bile reux and anastomotic strictures.
77,78
e most
FIGURE 22-11 Proximal dissection at the gastroesophageal
junction and diaphragmatic crura with en bloc removal of the gastric pericardial and paraesophageal lymph nodes.
Intestinal Reconstruction After Distal Gastrectomy
BILLROTH II RECONSTRUCTION
Given its technical ease, reasonable long-term patency rate, and good functional outcome, we generally recommend the
Chapter 22 Gastric Adenocarcinoma and Other Gastric Neoplasms (Except Gastrointestinal Stromal Tumors) 475
use of a Billroth II reconstruction after distal gastrectomy. is is achieved by identifying the jejunal origin at the ligament of Treitz, by tracing the Billroth II reconstruction distally to identify the shortest amount of jejunum necessary to create a tension-free anastomosis, roughly 15 cm from the ligament of Treitz. A shorter limb is thought to reduce the incidence of aerent limb syndrome. Once this point has been identied, it is marked with a suture to facilitate ease of future identication. Next, it must be decided whether to bring the jejunal limb to the proximal gastric remnant through a retrocolic or antecolic approach. Although there are advocates of both approaches, neither has been shown to have a true functional advantage over the other. We prefer the antecolic approach when the jeju­nal limb can easily reach in this manner, as it does not carry the attendant risk of retrocolic internal herniation. If limb length is an issue, the retrocolic approach may shorten the distance involved for a tension-free anastomosis. In this setting, we pre­fer to bring the gastric remnant down through the mesocolic defect so that the anastomosis is completely inframesocolic. is may reduce the incidence of aerent limb obstruction.
e gastrojejunal anastomosis is then created by placing the segment of the jejunal limb previously marked with suture adjacent to and in parallel with the proximal gastric remnant along its posterior-inferior margin. Once the location of the gastrojejunal anastomosis has been determined, a posterior row of Lembert-type sutures is placed to join the jejunum to the gastric wall. is is accomplished using either 3-0 Vicryl or silk-interrupted sutures along the entire posterior aspect
FIGURE 22-13 For a Billroth II anastomosis, a gastrojejunal anasto-
mosis is performed with a running absorbable monolament sutures.
of the anastomosis. Electrocautery is then used to create a full-thickness defect in the gastric wall anterior to the row of the posterior Lembert sutures that is long enough to facilitate a 5-cm anastomotic opening. A similar full-thickness defect is made in the adjacent segment of jejunum. An anastomosis is created using 3-0 or 4-0 PDS beginning at the posterior­middle segment. Two 3-0 PDS sutures are placed immedi­ately next to each other and run in opposite directions until they meet in the anterior aspect of the anastomosis. e two PDS sutures are then tied together to complete the anasto­mosis. Next, an anterior row of Lembert-type sutures are placed using either 3-0 Vicryl or silk suture (Fig. 22-13). If a retrocolic approach was used, the defect in the transverse mesocolon must be closed by sutures between the mesocolon and the stomach to avoid internal herniation.
ROUX-EN-Y RECONSTRUCTION
An acceptable alternative reconstruction method is Roux-en­Y gastrojejunostomy. e Roux technique has the advantage of eliminating bile reux into the gastric remnant but has the disadvantages of two anastomoses and the possibility of Roux­stasis syndrome. e Roux technique is approached by identi­fying the origin of the jejunum at the ligament of Treitz. e jejunum is traced distally to approximately 10–15cm. A defect is created in the jejunal mesentery just below the mesenteric border of the jejunum. e jejunum is then divided either between bowel clamps, or, as we prefer, with a gastrointesti­nal stapler (Fig. 22-14). e mesentery is divided enough to
FIGURE 22-14 For Roux-en-Y reconstruction, the jejunum is
divided 10–15 cm distal to the ligament of Treitz.
476 Part IV Stomach and Duodenum
permit the limb to reach to the gastric remnant while avoiding bowel devascularization. is usually includes division of the rst anastomotic arcade of the jejunum. Care should be taken with transillumination of the mesentery to understand the vascular anatomy and preserve blood supply to both limbs of the jejunum. e distal segment of the transected jejunum is brought to lie along the posterior-inferior aspect of the gastric margin as with the Billroth II reconstruction above. A poste­rior row of Lembert-type sutures is place to attach the jejunum to the gastric wall. is is accomplished using either 3-0 Vicryl or silk-interrupted sutures along the entire posterior aspect of the anastomosis. Electrocautery is then used to create a full­thickness defect in the gastric wall anterior to the row of the posterior Lembert sutures that is long enough to facilitate a 5-cm anastomotic opening. A similar full-thickness defect is made in the adjacent segment of jejunum. An anastomosis is created using 3-0 or 4-0 PDS beginning at the posterior­middle segment. Two 3-0 PDS sutures are placed immediately next to each other and run in opposite directions until they meet in the anterior aspect of the anastomosis. e two PDS sutures are then tied together to complete the anastomosis. Next, an anterior row of Lembert-type sutures are placed using either 3-0 Vicryl or silk suture (Fig. 22-15).
Attention is then turned to creation of the jejunojeju­nostomy. e proximal jejunal staple line is anastomosed to the distal jejunal segment approximately 45–50 cm distal to the gastrojejunostomy. is distance has previously been
shown to be the optimal length of the Roux limb needed to reduce the incidence of bile reux, while also reducing excessive limb length, which may contribute to stasis and malnutrition. e two segments of jejunum to be anasto­mosed are aligned parallel to each other in order to create a 5-cm antimesenteric anastomosis. e anastomosis may be
A
B
FIGURE 22-15 A. e distal segment of the transected jejunum is brought to lie along the posterior-inferior aspect of the gastric margin, and
a posterior row of Lembert type sutures is place to attach the jejunum to the gastric wall. B. Two 3-0 PDS sutures are placed immediately next to each other and run in opposite directions until they meet in the anterior aspect of the anastomosis. C. An anterior row of interrupted reinforcing Lembert suture is placed to complete the superior anastomosis.
C
Chapter 22 Gastric Adenocarcinoma and Other Gastric Neoplasms (Except Gastrointestinal Stromal Tumors) 477
reconstruction after distal gastrectomy with one notable vari­ation. Instead of creating a proximal gastrojejunostomy, the proximal anastomosis will be an end-to-end or end-to-side esophagojejunostomy. is may be performed as a hand-sewn anastomosis as described previously for a gastrojejunostomy or may be performed as a stapled technique using an appro­priately sized EEA stapler.
As described previously, the hand-sewn technique entails performing a circumferential reinforcing row of Lembert-type sutures using 3-0 Vicryl or silk. e posterior row is placed after aligning the anastomotic segments, ensuring the jejunal limb is not twisted. e anastomosis is then performed with two full-thickness 3-0 or 4-0 PDS sutures placed immedi­ately next to each other in the posterior segment of the anas­tomosis. e two sutures are then run circumferentially in opposite directions until they meet in the anterior midline. e sutures are then tied, completing the anastomosis. When feasible, an anterior row of interrupted reinforcing Lembert sutures are placed in the same manner as was completed in the posterior row (Fig. 22-17).
FIGURE 22-16 e two segments of jejunum to be anastomosed are
aligned parallel to each other, and a 5-cm antimesenteric anastomosis is created.
If a stapled technique is used, the anastomosis is created between the transected end of the esophagus and the antimes­enteric border of the proximal Roux limb near the staple line. e anastomosis is performed in and end-to-side fashion. e EEA sizers are placed in the esophageal lumen, choos­ing an anvil size that will allow the largest possible diameter
created with the use of a gastrointestinal stapler or may be hand-sewn in the same manner a described for the gastroje­junostomy above (Fig. 22-16). Care must be taken to close all mesenteric defects with either 3-0 Vicryl or silk to prevent the development of an internal hernia.
anastomotic lumen without causing undue tension on the esophageal or jejunal wall, preferably a 25- to 28-mm stapler. A purse-string suture is placed circumferentially at the distal end of the esophagus, just superior to the transection border using a 3-0 monolament suture. e anvil is placed in to the esophageal lumen, and the purse-string suture is tightened and tied snugly around the anvil rod. e stapled end of the Roux limb is opened, and the EEA stapler is placed through
Intestinal Reconstruction After Total Gastrectomy
the lumen in such a manner as to allow the staple pin to be punctured through the antimesenteric jejunal border several centimeters distally. e EEA anvil is then mated to the sta-
Total gastrectomy is associated with worse postoperative weight loss and increased dumping symptoms when compared to dis­tal gastrectomy. is is thought to be due to lack of a gastric reservoir. is has resulted in an ongoing debate of whether to create a jejunal pouch either with or without a jejunal interpo­sition technique in order to simulate the gastric reservoir func­tion. e literature in this area has generally been inconclusive due to the lack of appropriate controls, standardized outcomes
80–82
measures, and poor study design.
A recent meta-analysis and systematic review of the literature has provided level IA evidence to support the use of an inverted J pouch or S pouch in conjunction with a Roux-en-Y reconstruction as a means of improving postgastrectomy-associated dumping, long-term
78
weight loss, loss, and patient quality of life.
is study did not nd evidence to support the benet of a pouch with a jejunal interposition in order to maintain duodenal passage of enteric contents.
In most patients, a standard Roux-en-Y reconstruction will be the preferred technique to restore intestinal continuity. e procedure will be conducted as described previously for
pling device and closed, ensuring that the Roux limb is not twisted and no extraneous tissue is present between the anvil and stapler surface. Once stapling is completed, the device and anvil are removed through the jejunum and the stapler is inspected to ensure that the presence of two completed donuts of tissue are present (Fig. 22-18). e esophageal donut should be marked as “proximal esophageal margin” and sent to pathology for permanent section. e proximal end of the Roux limb must then be closed either with a surgi­cal stapler or hand-sewn technique.
Once the esophagojejunostomy has been performed, attention is turned to creation of the jejunojejunostomy as described for the Roux-en-Y technique for distal gastrectomy previously (Fig. 22-19).
For select patients who are thought to have a good long­term prognosis, use of a jejunal pouch should be consid­ered in an attempt to reduce postoperative weight loss and dumping syndrome. e jejunal S pouch or inverted J pouch are both reasonable choices, although no data exit to prove the benets of one over the other. e reconstruction
A
B
C
FIGURE 22-17 A–C. Roux-en-Y reconstruction with hand-sewn anastomosis after total gastrectomy.
478
Chapter 22 Gastric Adenocarcinoma and Other Gastric Neoplasms (Except Gastrointestinal Stromal Tumors) 479
A B
C
D
FIGURE 22-18 A–D. Roux-en-Y reconstruction with stapled anastomosis after total gastrectomy.
480 Part IV Stomach and Duodenum
FIGURE 22-19 Completed Roux-en-Y reconstruction after total
gastrectomy.
is performed just as a standard Roux-en-Y technique with the exception that the pouch is created at the proximal Roux limb prior to creating the esophagojejunostomy. e pouch is created by aligning the proximal jejunum in an inverted J or an S conguration, then by creating a common channel between the overlapping jejunal segments with a GIA stapler (Fig. 22-20). Once the pouch has been formed, a standard Roux-en-Y with esophagojejunostomy is performed as was described previously.
PRIMARY GASTRIC LYMPHOMA
Epidemiology
Gastric lymphoma is the second most common primary malignancy of the stomach, accounting for approximately 5% of gastric cancers. a nearly 80% increase in the incidence of lymphoma in the United States.
83
Over the past four decades, there has been
84
is marked increase in lymphoma incidence
A
FIGURE 22-20 A. Creation of a jejunal S pouch. B. Creation of
a jejunal J pouch.
B
has been especially notable for extranodal lymphomas, where up to 40% of cases present as primary gastrointestinal tract
85–87
lesions.
Gastric lymphoma accounts for the majority of
these cases, representing approximately 50–75 % of primary
83,88,89
gastrointestinal lymphomas.
Primary gastric lymphoma is typically an extranodal form of a non-Hodgkin’s lymphoma (NHL), whereas, Hodgkin’s lymphomas, are rarely found to involve the stomach.
83,90
Lymphomas represent a diverse and heterogeneous group of neoplasms and, as a result, have been very dicult to classify. Currently, the World Health Organization (WHO) lymphoma classication system is the accepted standard
91
used by most medical professionals worldwide.
is classi­cation system categorizes lymphomas based on their cell of origin and specic molecular, phenotypic, and genetic char­acteristics. Its most recent revision also takes into account clinical features such as patient age, site of involvement, and
92
associated etiologic conditions.
Although the WHO clas­sication system has facilitated treatment approaches and standardization of research protocols, it remains a very com­plex diagnostic schematic due to the intrinsic heterogeneity of lymphoproliferative disorders. e revised 2008 WHO lymphoma classication system recognizes more than 25 main categories of lymphoma derived from a mature B-cell origin and more than 20 derived from a T cell or NK cell of origin.
92,93
Chapter 22 Gastric Adenocarcinoma and Other Gastric Neoplasms (Except Gastrointestinal Stromal Tumors) 481
Histology
Histologically, up to 98% of primary gastric lymphomas are derived from a B-cell origin. classi ed as di use large B-cell lymphomas (DLBCL) and approximately 38% are marginal zone B-cell lymphomas of the mucosa-associated lymphoid tissue (MALT) ( Table
94
22-4 ).
Both DLBCL and MALT-associated B-cell lym-
phomas are thought to be associated with chronic H. Pylori infection.  is linkage is better established for MALT­associated B-cell lymphomas, where as many as 90% of cases are thought to be the result of H. pylori infection and where H. pylori eradication therapy usually leads to a dura-
95–98
ble remission.
 e association between H. pylori infec-
tion and DLBCL is more controversial. Approximately 35% of patients with DLBCL are found to be H. pylori posi- tive, with the majority of these patients showing concurrent MALT areas on endoscopic evaluation. Despite these data, up to 63% of patients with DLBCL have a durable treat­ment response to H. Pylori eradication therapy alone.
Di use large B-cell lymphomas are aggressive high-grade
lymphomas that may be derived from MALT-associated B-cell
87,
lymphomas.
88 Di use large B-cell lymphomas frequently
express high levels of Bcl-6, an oncogene found on chromo-
83
some 3.
 ere are two recognized subcategories of DLBCL that can be immunohistochemically di erentiated: those that resemble germinal center (GC)–type B cells (CD10+, Bcl-6–, and BCL2+/–) and those that are not GC-like (CD10–, Bcl-
83
6+, and BCL2–).
GC-type B cells are thought to be derived de novo from mature B lymphocytes, while non–GC-type DLBCL is thought to arise from MALT-associated B-cell lymphomas.
MALT-associated B-cell lymphomas are typically
multifocal lesions.  ey arise from gastric mucosal lymphatic tissue, which is thought to occur as a result of chronic H. pylori infection, in most cases. MALT-associated B-cell lymphomas express the CD20 cell surface antigen, generally produce IgG light-chain antibodies, and may express CD43.  ree genetic translocations have been identi ed for MALT- associated
TABLE 22-4: DISTRIBUTION OF LYMPHOMA
HISTOLOGICAL SUBTYPE IN 398 PATIENTS WITH PRIMARY GASTRIC LYMPHOMA (REAL CLASSIFICATION) 94
Lymphoma Histological Distribution Frequency (%)
Di use large B-cell lymphoma 59 Without MALT component 14 With MALT component 45 Malt lymphoma of the marginal zone 38 Peripheral T-cell lymphoma 1.5 Mantle lymphoma 1 Follicular lymphoma 0.5
MALT, mucosa-associated lymphoid; REAL, Revised European-American Lymphoma.
93
Nearly 60% of these are
98
B-cell lymphomas that, when combined, may be present in up to 65% of cases.  ese characteristic translocations include t(11;18)(q21;q21), t(1;14)(p22;q32), and t(14;18)
83,
(q32;q21).
98 Although each of these translocations produces a di erent direct upstream impact on cellular regulation, they all result in activation of the nuclear factor-kB cell activation
99
pathway.
Sings and Symptoms
 e clinical presentation of patients with primary gastric lymphoma is similar to patients with gastric adenocarcinoma.  e signs and symptoms tend to be nonspeci c, with dyspep­sia, abdominal pain, nausea, vomiting, anorexia, and change
83,
91,
98,
100
in bowel habits being the most common.
Gastroin-
testinal bleeding may also occur and is the initial presentation
88
in up to 30% of patients.
With the exception of weight loss,
B symptoms (weight loss, fevers, and night sweats) are rarely
83
present in primary gastric lymphomas.
A complete history and physical examination must be performed with particular emphasis paid to examination of all accessible nodal beds, including Waldeyer’s ring. A detailed abdominal examination should be performed to evaluate for an abdominal masses or organomegaly.  e patient’s presenting history provides the most important diagnostic clues, as the physical examination will fail to reveal any diagnostic  ndings up to 60% of the
83
time.
Diagnostic Workup and Staging
Patients with presenting histories or objective  ndings on clinical examination concerning for gastric malignancy must be undergo immediate upper endoscopic evaluation. Com­prehensive upper endoscopy with biopsy of concerning lesions will make the diagnosis of gastric lymphoma in more than 95% of cases. has been pathologically con rmed, the patient must undergo staging of their disease to ensure initiation of the appropriate treatment algorithm and provide the patient with prognos­tic information. Although nearly universal acceptance of the 2008 WHO lymphoma classi cation system has helped to standardize the lymphoma staging workup, some variations still exist depending on the histological subtype.
All patients should undergo laboratory testing to include
H. Pylori serology, a CBC with di erential, liver function tests, serum chemistry panel with lactate dehydrogenase (LDH)
microglobulin, and serum electrophoresis to evaluate
and B
2
for M proteins. Additionally, although the bone marrow is rarely involved in primary gastric lymphoma, a bone marrow aspirate and biopsy should be completed. A spiral CT scan of the neck, chest, abdomen, and pelvis is performed to evaluate for addition lesions. by pathological analysis, a PET scan has been demonstrated to increase staging accuracy above that of CT scan alone with a sensitivity of more than 80% and a speci city of more than
91
Once the diagnosis of gastric lymphoma
91,
99 When DLBCL has been conformed