General Data. Age: 75y/o Sex: female Date of admission:

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Transcription:

General Data Age: 75y/o Sex: female Date of admission: 87-10-31

Chief complaint Poor oral intake, hunger pain for months and body weight loss about 10kg in 3 months

Present Illness Quit healthy before DM(-), HTN(-), CVD(-), smoking(-), drinking(-) 3 months ago, LLQ abdominal discomfort, poor appetite noted PES and colonoscopy done in Argentina -- Polyps noted -- Biopsy: unknown finding

Present Illness 1 month ago, intermittent LLQ abdominal pain, upper abdominal pain (hunger pain and relieved after meal) and vomiting noted Body weight loss: 10kg in 3 months

PE GA: fair Con s: clear Vital sign: TPR:36.4/90/17, BP:120/78mmHg HEENT: conjunctivae: pale LAP(+) about 1x1cm in size at left post-scm area Chest: breathing sounds: clear heart sounds: regular, no murmur Abdomen: flat and soft, LLQ tenderness bowel sounds: hypoactiv Extremities: freely movable, pitting edema(+)

Impression Peptic ulcer Poor oral intake and body weight loss suspect malignancy induced

Evaluation 11-1 Hb: 7.9, MCV: 79.1, Ret%:1.5% WBC: 8440, Seg: 86.8%, Plt: 624000 11-2 Albumin:2.1, GOT:28, GPT:34 BUN:8.6, Cr:0.7 Fe:1, TIBC:195 11-3 CEA: 1.39 (0~4.6), AFP: 1.13 (0~15), CA125: 48.22 (10~35)

Evaluation 11-3 PES: A very big ulcerating tumor with infiltrating margin was found at cardia to angle. Biopsy x 4 IMP: carcinoma, advanced, stomach, with extension to esophagus

Evaluation 11-3 Abdominal Sonar: multiple hypoechoic nodule (1~2cm) were noted near pancreatic head & aorta. IMP: chronic parenchymal liver disease, liver sludge, thicken GB wall, hypoechoic lesions, nature? r/o LN enlargement

Evaluation 11-6 Hb:11.7 (PRBC:4U) 11-6 Abdomen CT 11-9 UGI series 11-16 Small bowel series 11-18 Patient transfer to 和信 Hospital for C/T

UGI

UGI

CT Pleura effusion Thickened esophageal wall

CT

CT Thickened gastric wall Soft tissue density at the lesser sac Liver intact

CT

CT Soft tissue density at retroperitonium

CT

CT Soft tissue density at peri-aortic area near pelvic inlet

CT Impression: 1. Lymphoma 2. Gastric cancer with lymphatic metastasis

Pathology Stomach & Esophagus biopsy Malignant lymphoma made up of large-sized atypical lymphoid cells, B cell Diffuse infiltrating in the esophagus and gastric tissue

Diagnosis Gastric lymphoma, Diffuse large B cell type malignant lymphoma from cardia to angle

Differential Diagnosis

Gastric maliganancies The stomach is the site of variety of malignant neoplasms. They are primary carcinoma, gastric lymphoma, mesenchymal tumours and metastatic carcinomas. The most common of these are carcinoma and lymphoma.

Gastric carcinoma: Morphology Primary carcinoma of the stomach may be present as: 1. Superficial spreading carcinoma (Early gastric cancer) Type I lesions are elevated and protrude more than 5 mm into the lumen. Type II tumors are superficial lesions that are elevated (IIa), flat (IIb), or depressed (IIc). Type III early gastric cancers are shallow, irregular ulcers surrounded by nodular, clubbed mucosal folds.

Gastric carcinoma: Morphology 2. Polypoid or fungating carcinoma 3. Ulcerating or penetrating carcinoma (70%) 4. Advanced bulky carcinoma 5. Infiltrating or cirrhous carcinoma (5~15%) (linitis plastica)

Gastric carcinoma: UGI 1. Superficial spreading carcinoma a flat or slightly depressed lesion accompanied by converging folds 2. Polypoid or fungating carcinoma irregular protruding mass 3. Ulcerating or penetrating carcinoma ulcerated mass, amputation of folds surface may be highly irregular (cauliflower)

Gastric carcinoma: UGI 4. Advanced bulky carcinoma mass or bulk, one or more ulceration, irregular surface, margins may be a distinct angular demarcation (shelf) 5. Infiltrating or cirrhous carcinoma (linitis plastica) fibrotic reaction, contracted stomach lacking the normal rugal fold pattern with a smooth or a finely granular surface

Gastric carcinoma: CT thickening of the gastric wall, asymmetric thickening of folds, irregular nodular luminal surface, mass of uniform density

Gastric carcinoma: Spread 1. beyond the serosa, obliteration of the pre-gastric fat planes 2. direct extension to adjacent structures including the oesophagus, gastrocolic ligament, gastrohepatic ligament, gastrosplenic ligament and pancreas. 3. Further extension may involve any of the lymph node groups in the upper abdominal region. 4. The most common sites of distant metastases are the liver and peritoneal cavity

Gastric lymphoma Radiographic type: 1. Polypoid or nodular (47%) enlarged nodular folds 2. Ulcerative (42%) ulcerative lesions, may be complicated by perforation; aneurysmal configuration 3. Diffusely infiltrating(11%) diffuse hoselike thickening of bowel; decreased or absent peristalsis

Gastric lymphoma: UGI 1. Infiltrative, ulcerative, or nodular mass that often mimics the appearance of adenocarcinoma. Flexibility of gastric wall preserved. 2. The antrum and body are most commonly involved. Duodenum often affected when antrum involved. 3. Circumscribed mass with endogastric or exogastric growth 4. Large irregular ulcers

Gastric lymphoma: CT 1. diffuse involvement of entire stomach, typically more than half of gastric circumference 2. segmental involvement 3. thickened gastric wall 4. luminal irregularity, hyperrugosity 5. spread of the tumour: direct extension into pancreas, spleen, transverse colon and liver

Discussion Gastric Lymphoma

Lymphoma Hodgkin (1) non-hodgkin (10~15) Presentation Usually nodal Usually extranodal Spread Contiguous Hematogenous, Non-contiguous Mediastinum Common Uncommon(except lymphoblastic type) Spleen Common Uncommon Bone Marrow Uncommon Liver,GI,CNS Uncommon Common Common

Gastric Lymphoma Primary gastric lymphomas: less than 2% of all primary stomach malignancies Non Hodgkin's type and of B-cell lineage almost 75% of primary gastrointestinal lymphomas were of gastric origin. Gastric lymphomas are more prevalent in patients over the age of 50, and men are affected two to three times more frequently than women

Gastric Lymphoma Usually arise from MALT (mucosa associated lymphoid tissue)- also known as Marginal Zone B-cell lymphoma (Low and High grade). Diffuse large B-cell lymphoma include high grade lymphoma of MALT origin and non- MALT type and they are indistinguishable

MALToma Stomach, Mucosa associated lymphoid tissue Related to H. pylori Low grade, remission after H. pylori eradication Other sites: lung, breast, salivary gland, lacrimal gland

Gastric Lymphoma: Clinical Sign Most common: abdominal pain, nausea and vomiting, anorexia, weight loss, and bleeding. Early symptoms are vague. More advanced lesions may present with weakness, hemorrhage, pyloric stenosis, or signs of perforation. PE:Abdominal tenderness(35%), a palpable abdominal mass(20-30%), hepatomegaly(14%)

Gastric Lymphoma: Staging Ann Arbor staging system Stage IE: tumor confined to the GI tract Stage IIE: regional lymph node involvement Stage IIIE: spread to other organs within the abdomen Stage IV: spread beyond the abdomen

Gastric Lymphoma: Prognosis IPSS (International prognostic scoring system; for Diffuse large B cell lymphoma initially) 1. Age>60y/o 2. Ann Arbor stage ⅢorⅣ 3. Extranodal involvement >1 site 4. Poor performance status (ECOG 2~4) 5. High LDH Risk: low(<1), low-intermediate(2), intermediate-high(3), high(4~5)

Gastric Lymphoma: Treatment Surgery: 1. No decrease in survival for patients if adjuvant RT or C/T were given than total resection of all gross disease and involved lymph nodes. 3. In surgically treated patients, most recurrences are extraabdominal and local disease is well controlled. 4. Currently, splenectomy is only indicated in cases of direct tumor extension.

Gastric Lymphoma: Treatment Radiotherapy: Gastric lymphoma seems to be a more systemic disease with the majority of recurrences occurring at extraabdominal sites. So, in the absence of obvious persistent local disease, the need for additional local therapy with RT is put in question.

Gastric Lymphoma: Treatment Chemotherapy: 1. As stated earlier, most primary gastric lymphomas are of the diffuse histiocytic or the diffuse large cell type. They are quite responsive to current chemotherapy. 2. Stages IE & IIE treated with chemotherapy after surgery: excellent 5-year disease free survival

Gastric Lymphoma: Treatment C/T regimens: CHOP (cyclophosphamide, Adriamycin, vincristine, prednisone) CHOP-bleo (added bleomycin) COPP-bleo (cyclophosphamide, vincristine, procarbazine, prednisone, bleomycin) CVP (cyclophosphamide, vincristine, and prednisone)

Gastric Lymphoma: Treatment C/T High grade Aggressive course without tratment 80% complete remission rate by C/T 40% cure by C/T Low grade Indolent course even late stage Incurable by C/T

Gastric Lymphoma: Treatment Conclusion: Early stage: Surgery: for local control and preoperative staging Adjuvant C/T: for extraabdominal lesion

Gastric Lymphoma: Treatment Conclusion Invasion: C/T: mainstay of treatment with either surgery or radiation providing local control. In those patients with non-diagnostic biopsies, surgical exploration and resection are needed.