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1.
Jpn J Clin Oncol ; 29(2): 106-8, 1999 Feb.
Article in English | MEDLINE | ID: mdl-10089952

ABSTRACT

We describe a case of advanced esophageal cancer treated successfully by chemotherapy with nedaplatin alone. A 60-year-old male with type 2 advanced esophageal cancer, which was located in the upper part of the esophagus and had invaded adjacent organs, was treated with nedaplatin 150 mg/body (100 mg/m2) given intravenously every 4 weeks from January 6, 1991. He achieved a partial response (PR) and was discharged in March 1991. Subsequently, he received nedaplatin 75 mg/body in an out-patient setting almost every month until August 1992. Toxicities were tolerable and included mild thrombocytopenia and nausea/vomiting. From serial evaluation in October 1993, the esophageal tumor was not observed. After 7 years since initial chemotherapy was administered, he still survives without the disease.


Subject(s)
Antineoplastic Agents/therapeutic use , Carcinoma, Squamous Cell/drug therapy , Esophageal Neoplasms/drug therapy , Organoplatinum Compounds/therapeutic use , Antineoplastic Agents/administration & dosage , Carcinoma, Squamous Cell/diagnostic imaging , Carcinoma, Squamous Cell/pathology , Disease-Free Survival , Drug Administration Schedule , Esophageal Neoplasms/diagnostic imaging , Esophageal Neoplasms/pathology , Esophagoscopy , Humans , Infusions, Intravenous , Male , Middle Aged , Organoplatinum Compounds/administration & dosage , Radiography
2.
Gan To Kagaku Ryoho ; 24(7): 879-82, 1997 May.
Article in Japanese | MEDLINE | ID: mdl-9170530

ABSTRACT

We reported two cases of advanced gastric cancer effectively treated with chemotherapy of 5-fluorouracil (5-FU), cisplatin (CDDP) and cytarabine (Ara-C), 5-FU (300-350 mg/body) was given by continuous intravenous infusion. Ara-C (20-40 mg/body) by continuous infusion and CDDP (15-20 mg/body) were added intravenously for 3-6 days. For case 1, epirubicin (30 mg/body) was also given on the first day of each therapy course. Case 1 was a 62-year-old female who had gastric cancer with liver metastasis, ovarian metastasis and peritonitis carcinomatosa. After 3 courses of the chemotherapy, reduction of ovarian metastasis greater than 75% was observed. The value of CA125 decreased from 6,800 U/ml to 527 U/ml and ascites disappeared. Case 2 was a 54-year-old male who had type 3 advanced gastric cancer with multiple liver metastases. He received 6 courses of the therapy. Both primary and metastatic tumors showed over 50% reduction in tumor size. These suggested that this combination therapy was effective for inoperable advanced gastric cancers.


Subject(s)
Adenocarcinoma/drug therapy , Antineoplastic Combined Chemotherapy Protocols/therapeutic use , Stomach Neoplasms/drug therapy , Cisplatin/administration & dosage , Cytarabine/administration & dosage , Drug Administration Schedule , Female , Fluorouracil/administration & dosage , Humans , Male , Middle Aged
4.
Pathol Res Pract ; 191(11): 1165-7, 1995 Nov.
Article in English | MEDLINE | ID: mdl-8822120

ABSTRACT

A 72 year old female was admitted for an operation of gastric cancer. At the operation, a 3 x 3 cm-sized, whitish and multilocular nodule was incidently found at the left side of the spleen. This nodule was adjoining the splenic capsule and was characterized with sparsely found multilocular lymphatic cysts with varying sizes. The walls of these cysts were composed of partly thin fibrous tissue, or partly thin to thick splenic trabeculae. Abnormally elongated, nodular or fragmentary trabeculae were also present in the nodule. White and red splenic pulp was found widely dispersed among the cysts. The surrounding splenic tissue was not compressed. We considered the essence of this tumor to be an abnormal mixture of normal splenic elements such as lymphatics, splenic trabeculae, and red and white pulp, and regarded this tumor as a focal malformation (lymphangiomatous hamartoma) rather than a true neoplasm such as a lymphangioma.


Subject(s)
Castleman Disease/pathology , Lymphangiectasis/pathology , Lymphangioma/pathology , Splenic Diseases/pathology , Splenic Neoplasms/pathology , Aged , Diagnosis, Differential , Female , Humans
5.
Mod Pathol ; 7(3): 416-21, 1994 Apr.
Article in English | MEDLINE | ID: mdl-8058718

ABSTRACT

A case of glycogen storage disease associated with multiple hepatic adenomas and Niemann-Pick disease is reported. Type IA glycogen disease was diagnosed soon after birth in a female patient, and she was treated at our clinic. At the age of 12 yr, the patient was found to have a hepatic tumor, which was surgically extirpated. Histological examination showed that the tumor was a hepatocellular adenoma. Increasing hepatomegaly and jaundice were noted when the patient was 18 yr of age. She died of pneumonia and cardiac tamponade at the age of 19. The liver weighed 3310 g, and showed severe jaundice and many nodules measuring up to 8 cm in diameter. These nodules were composed of mature hepatocytes without atypia and were diagnosed as hepatocellular adenomas. In addition, many adenomatous lesions were found at the microscopical level. The spleen weighed 1310 g, and showed two small infarctions at the upper part. A histological examination showed a diffuse infiltration of large foamy cells in the splenic red pulp. These cells were 20 to 100 microns in diameter and weakly positive for periodic acid-Schiff (PAS) staining, positive for lipid staining with Sudan black B, and positive for Pearce's phospholipid staining. Electron microscopy showed many lamellar bodies in the cytoplasm that were characteristic of Niemann-Pick disease. These foamy cells were also found in liver, bone marrow, lymph nodes, kidneys, and lungs.(ABSTRACT TRUNCATED AT 250 WORDS)


Subject(s)
Glycogen Storage Disease Type I/complications , Lipids/analysis , Niemann-Pick Diseases/complications , Sphingomyelin Phosphodiesterase/metabolism , Adenoma/complications , Adenoma/metabolism , Adenoma/pathology , Adult , Fatal Outcome , Female , Glycogen Storage Disease Type I/metabolism , Glycogen Storage Disease Type I/pathology , Humans , Liver Neoplasms/complications , Liver Neoplasms/metabolism , Liver Neoplasms/pathology , Niemann-Pick Diseases/metabolism , Niemann-Pick Diseases/pathology
6.
J Gastroenterol ; 29(2): 199-202, 1994 Apr.
Article in English | MEDLINE | ID: mdl-8012509

ABSTRACT

Tightly coiled spiral micro-organisms (Gastrospirillum hominis), distinct from Helicobacter pylori, were found in the gastric mucosa of a 66-year-old man with a 4-month history of intermittent epigastric pain. The organisms were distributed in the antral mucosa, which showed erosive gastritis; histologically, the affected mucosa presented moderate to severe chronic gastritis with focal neutrophil infiltration. After a 2-week administration of cimetidine, his symptoms resolved and the active inflammation was reduced, both endoscopically and histologically, but the organisms still remained. Biopsy specimens taken 4 weeks after treatment with minocycline and cimetidine showed normal gastric mucosa without the spiral organisms. The above clinical course suggests the possible role of Gastrospirillum hominis in the pathogenesis of gastritis.


Subject(s)
Bacterial Infections , Gastritis/microbiology , Helicobacter heilmannii/isolation & purification , Aged , Cimetidine/therapeutic use , Gastric Mucosa/microbiology , Gastric Mucosa/pathology , Gastritis/drug therapy , Gastritis/epidemiology , Humans , Japan/epidemiology , Male , Minocycline/therapeutic use
7.
Acta Pathol Jpn ; 43(12): 779-82, 1993 Dec.
Article in English | MEDLINE | ID: mdl-8109256

ABSTRACT

An autopsy case of a hepatocellular carcinoma (HCC) with unusual metastasis to the mucosa of the small intestine is reported. The patient was a 73 year old female. At autopsy, the liver weighed 970 g, and an ovoid and necrotic 6 x 5 cm sized tumor was found in the right posterior lobe with many daughter tumors within the cirrhotic liver. The tumor embolus in the portal vein was not found. Extrahepatically the tumor metastasized to the lungs, sacral bone and hepatohillar and para-aortic lymph nodes. Additionally, many sessile and pedunculated polyps up to 2 cm in diameter were found sporadically in the small intestine. These seemed to be primary adenomatous polyps but histologically they were HCC metastasis. To the best of the authors' knowledge, many polypoid involvements of the small intestine by a hepatocellular carcinoma have not been reported until now.


Subject(s)
Carcinoma, Hepatocellular/secondary , Intestinal Neoplasms/secondary , Intestinal Polyps/secondary , Liver Neoplasms/pathology , Aged , Carcinoma, Hepatocellular/pathology , Female , Humans , Intestinal Neoplasms/pathology , Intestinal Polyps/pathology
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