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1.
Gan To Kagaku Ryoho ; 50(2): 191-193, 2023 Feb.
Article in Japanese | MEDLINE | ID: mdl-36807169

ABSTRACT

A 74-year-old woman with severe anemia was presented to our hospital to investigate the cause of the disease. Under investigation, submucosal tumor in the small intestine was suspected. We performed the laparoscopic surgery for resection. The pathological diagnosis was dedifferentiated liposarcoma originated from the small bowel mesentery.


Subject(s)
Laparoscopy , Liposarcoma , Peritoneal Neoplasms , Female , Humans , Aged , Liposarcoma/surgery , Mesentery/pathology , Mesentery/surgery , Neoplasm Recurrence, Local/surgery , Peritoneal Neoplasms/surgery
2.
Intern Med ; 62(14): 2093-2098, 2023 Jul 15.
Article in English | MEDLINE | ID: mdl-36476548

ABSTRACT

A 60-year-old Japanese man diagnosed with acromegaly at 28 years old had difficulty walking due to worsening back pain. He had been treated with somatostatin analog since 57 years old, but his pain and numbness continued to worsen. Lumbar magnetic resonance imaging showed disc bulging at L3/4 and L4/5, and he was diagnosed with lumbar spinal canal stenosis due to hypertrophy of the yellow ligament. Patients with acromegaly may complain of osteoarthropathy, so we must pay attention to the symptoms of spinal canal stenosis in collaboration with orthopedic specialists.


Subject(s)
Acromegaly , Spinal Stenosis , Male , Humans , Adult , Middle Aged , Acromegaly/complications , Acromegaly/diagnosis , Constriction, Pathologic , Lumbar Vertebrae/diagnostic imaging , Spinal Stenosis/complications , Spinal Stenosis/diagnostic imaging , Back Pain , Magnetic Resonance Imaging , Spinal Canal/diagnostic imaging
3.
Intern Med ; 61(22): 3377-3381, 2022 Nov 15.
Article in English | MEDLINE | ID: mdl-35491130

ABSTRACT

Primary cardiac lymphomas (PCLs) are extremely rare tumors with a poor prognosis. They usually involve the pericardium and the right side of the heart. PCLs arising from the left side of the heart are relatively rare, with bilateral cases being even rarer. We herein report a case of PCL arising from both the right and left sides of the heart in a 65-year-old man. Multiple imaging modalities clearly demonstrated the tumors at the initial evaluation. The pathological diagnosis was diffuse large B-cell lymphoma.


Subject(s)
Heart Neoplasms , Lymphoma, Large B-Cell, Diffuse , Male , Humans , Aged , Heart Neoplasms/diagnosis , Lymphoma, Large B-Cell, Diffuse/diagnosis , Lymphoma, Large B-Cell, Diffuse/diagnostic imaging , Pericardium/pathology
4.
Gan To Kagaku Ryoho ; 48(7): 955-957, 2021 Jul.
Article in Japanese | MEDLINE | ID: mdl-34267035

ABSTRACT

The case involved a 51-year-old woman who was diagnosed with Stage Ⅰ right breast cancer(cT1, N0, M0). Partial resection of the right breast and sentinel lymph node biopsy were performed. The histological type was found to be Stage Ⅰ triple-negative medullary carcinoma with pT1c, pN0(sn), and M0. A pituitary tumor was diagnosed after discharge. After removal of the pituitary tumor, whole-breast irradiation was performed. Subsequently, chemotherapy was started. Approximately 5 months after surgery, redness and swelling of the right breast were observed. Inflammatory breast cancer recurrence could not be ruled out by imaging, and skin biopsy was performed. No malignant findings were observed, and the symptoms were considered to indicate radiation recall dermatitis caused by chemotherapy. When chemotherapy was discontinued, the redness of the right breast improved.


Subject(s)
Breast Neoplasms , Inflammatory Breast Neoplasms , Radiodermatitis , Axilla , Breast Neoplasms/surgery , Female , Humans , Inflammatory Breast Neoplasms/diagnosis , Middle Aged , Neoplasm Recurrence, Local/surgery , Radiodermatitis/diagnosis , Radiodermatitis/etiology , Sentinel Lymph Node Biopsy
5.
Am J Case Rep ; 21: e922405, 2020 Mar 24.
Article in English | MEDLINE | ID: mdl-32205837

ABSTRACT

BACKGROUND Strangulation ileus is caused by external obstruction to the small bowel, which results in ischemia and loss of bowel peristalsis. Low-grade appendiceal mucinous neoplasm (LAMN) is a low-grade adenocarcinoma that arises in the appendix. LAMN is usually asymptomatic but can present with appendiceal rupture and pseudomyxoma peritonei (PMP). This report is of a rare presentation of LAMN with strangulation ileus in a 92-year-old man. CASE REPORT A 92-year-old man was admitted to the emergency room with sudden onset of lower abdominal pain and abdominal distension. Laboratory investigations showed a leukocytosis with a white blood cell (WBC) count of 14.6×10³/µL with 85.5% neutrophils, blood urea nitrogen (BUN) of 26.6 mg/dL, and serum creatinine of 2.6 mg/dL, consistent with acute renal failure. Arterial blood gas analysis showed lactic acidosis (pH of 7.11) with a base excess of -20.8 mmol/L and lactate of 13.7 mmol/L. Abdominal computed tomography (CT) showed ascites and a dilated obstructed closed loop of the distal ileum associated with an external mass (3.9×2.8 cm). An initial diagnosis was of strangulation ileus due to Meckel's diverticulum. Emergency ileocecal resection was performed. Histopathology showed a low-grade mucinous tumor arising from the mucosa of the appendix, consistent with LAMN. At a 13-month follow-up, the patient was well with no tumor recurrence. CONCLUSIONS This report is of a rare case of LAMN that presented as a surgical emergency with strangulation ileus.


Subject(s)
Adenocarcinoma, Mucinous/complications , Appendiceal Neoplasms/complications , Ileus/etiology , Meckel Diverticulum/etiology , Adenocarcinoma, Mucinous/surgery , Aged, 80 and over , Appendiceal Neoplasms/surgery , Emergency Service, Hospital , Humans , Ileus/surgery , Male , Meckel Diverticulum/surgery , Treatment Outcome
6.
Hinyokika Kiyo ; 65(4): 117-121, 2019 Apr.
Article in Japanese | MEDLINE | ID: mdl-31247689

ABSTRACT

The patient was a 56-year-old female. She was referred to our department for further examination of right hydronephrosis in 2010. Computed tomography (CT) showed right hydronephrosis, and retrograde pyelography (RP) revealed stenosis of the right lower ureter. Urine cytology was negative. Transurethral biopsy of the right ureter was performed using ureteroscopic cup forceps and the histopathlogical diagnosis was ureteral amyloidosis. A whole-body search was performed, including rectal biopsy, but no evidence of amyloidosis was obtained. She was diagnosed with localized amyloidosis of the right ureter. A ureteral stent was indwelled and the patient was given occulusive dressing technique (ODT) therapy using dimethyl sulfoxide (DMSO) for 1 year. After ODT therapy, right hydronephrosis improved. After a 2-year followup, it worsened. ODT therapy was restarted and continued for 2 years. She consulted our department because of fever and right lumbago in April 2017 after a 4-month interruption of ODT therapy. CT revealed progression of the right hydronephrosis. A ureteral stent was indwelled and ODT therapy was restarted. The right hydronephrosis improved after 1 year. ODT therapy using DMSO was effective for localized ureteral amyloidosis, but periodic follow-up was necessary and ODT therapy was also effective when it recurred after the interruption of treatment.


Subject(s)
Amyloidosis , Dimethyl Sulfoxide , Free Radical Scavengers , Ureter , Ureteral Diseases , Amyloidosis/drug therapy , Bandages , Dimethyl Sulfoxide/therapeutic use , Female , Follow-Up Studies , Free Radical Scavengers/therapeutic use , Humans , Middle Aged , Ureteral Diseases/drug therapy
7.
Nihon Shokakibyo Gakkai Zasshi ; 116(3): 256-264, 2019.
Article in Japanese | MEDLINE | ID: mdl-30853679

ABSTRACT

We herein report a rare case of autoimmune pancreatitis with small intestinal obstruction. A 72-year-old male was admitted to our hospital with abdominal fullness and vomiting and diagnosed with autoimmune pancreatitis by imaging and laboratory tests. Imaging studies also revealed narrowing of the proximal jejunum with dilated bowels and intramural cystic lesion adjacent to the pancreatic body. Small bowel resection was performed to alleviate stenosis. Pathological evaluation demonstrated invasion of IgG4-positive cells and fibrosis.


Subject(s)
Autoimmune Diseases/diagnosis , Constriction, Pathologic/diagnosis , Intestinal Obstruction/diagnosis , Pancreatitis/diagnosis , Aged , Humans , Male , Pancreas , Pancreatitis/immunology
8.
Nihon Hinyokika Gakkai Zasshi ; 110(1): 22-27, 2019.
Article in Japanese | MEDLINE | ID: mdl-31956214

ABSTRACT

Three cases are reported of TURBT on the anterior wall, with bladder rupture occurring after discharge. Patient 1 was a 68-year-old man. He had macroscopic hematuria and he strained to void a bloody clot on the 10th day after TURBT. Subsequently, right lower abdominal pain occurred. Computed tomography (CT) revealed the extravasation of contrast medium into the prevesical space. He was diagnosed with extraperitoneal bladder rupture, and a urethral catheter was indwelled. Cancer invasion of muscle was diagnosed by pathological examination and total cystectomy was scheduled one and a half months later, but the prostate could not be resected due to hard tissue around the bladder neck. Patient 2 was an 82-year-old man and had a history of radiation therapy for a muscle invasive bladder tumor. He complained of pollakisuria two weeks after TURBT, and renal failure was detected on a blood test. CT revealed ascites, and a urethral catheter was indwelled. Ascites disappeared, but the urethral catheter deviated into the abdominal cavity based on repeated CT the next day, and he was diagnosed with intraperitoneal bladder rupture. Emergent surgery was performed, and the ruptured part was sutured with omentum covering and a cystostomy was created. Patient 3 was an 83-year-old man undergoing treatment for benign prostatic hypertrophy (BPH). He had received bladder instillation therapy of Bacillus Calmette-Guerin (BCG) ten months previously. When urinating 6 days after TURBT, lower abdominal pain developed. CT demonstrated retroperitoneal bladder rupture, and a urethral catheter was indwelled. The urethral catheter was removed 6 days later, but lower abdominal pain occurred again the next day. Thus, the urethral catheter was re-indwelled for a further two weeks.In TURBT on the anterior wall or dome, for the patients who had previously received radiation therapy to the pelvis, or intravesical instillation therapy of the BCG or accompanied by urinary disturbance, such as BPH, it is necessary to consider bladder rupture after discharge.


Subject(s)
Postoperative Complications , Urinary Bladder Neoplasms/surgery , Urinary Bladder/surgery , Aged , Aged, 80 and over , Humans , Male , Rupture, Spontaneous
9.
Taiwan J Obstet Gynecol ; 57(3): 449-451, 2018 Jun.
Article in English | MEDLINE | ID: mdl-29880183

ABSTRACT

OBJECTIVE: Spontaneous pneumothorax combined with thoracic endometriosis is a rare condition during pregnancy. We present a case of chemical pleurodesis with autologous blood and freeze-dried concentrated human thrombin during pregnancy. CASE REPORT: This report presents a case of spontaneous pneumothorax combined with thoracic endometriosis that arose at 22 weeks' gestation in a 35-year-old female. The initial chest drainage was unsuccessful. At 25 weeks' gestation, video-assisted thoracoscopic surgery was performed and revealed endometriosis in the thoracic cavity. Since the leak persisted, chemical pleurodesis was performed with autologous blood and freeze-dried concentrated human thrombin at 28 weeks' gestation. The leak improved markedly and did not recur. CONCLUSION: This is the first case report about chemical pleurodesis with autologous blood and freeze-dried concentrated human thrombin during pregnancy. This procedure might contribute to the management of pneumothorax in pregnant women.


Subject(s)
Blood Transfusion, Autologous , Hemostatics/administration & dosage , Pleurodesis , Pneumothorax/therapy , Pregnancy Complications/therapy , Thrombin/administration & dosage , Adult , Endometriosis/complications , Endometriosis/diagnosis , Female , Humans , Pneumothorax/complications , Pneumothorax/diagnostic imaging , Pneumothorax/surgery , Pregnancy , Thoracic Diseases/complications , Thoracic Diseases/diagnosis , Thoracic Surgery, Video-Assisted
10.
Hinyokika Kiyo ; 64(4): 165-168, 2018 Apr.
Article in Japanese | MEDLINE | ID: mdl-29772618

ABSTRACT

The patient was an 88-year-old male. He was referred to the Department of Internal Medicine because of total body itching and jaundice in July 2011. The serum bilirubin level was elevated, and the serum CA19-9 level was also elevated to 266. 6 U/ml. Computed tomography (CT) and endoscopic retrograde cholangiopancreatography (ERCP) revealed a solid tumor between the hepatic hilus and common bile duct, and choler cytodiagnosis was class V ; adenocarcinoma. The patient was diagnosed with hilar cholangiocarcinoma and received conservative treatment with endoscopic nasobiliary drainage (ENBD) due to his advanced age. The patient was then referred to our department because CT revealed right hydronephrosis and thickening of the right side of the bladder wall, which had not been detected on admission in October 2011. Cystoscopy revealed a broad-based edematous tumor on the right side of the bladder. Transurethral resection of the bladder tumor (TURBT) was performed. The histological diagnosis was moderately differentiated tubular adenocarcinoma. Immunohistostaining using CA19-9 was performed, and cancer cells were positive. The final histology led to a diagnosis of metastasis of cholangiocarcinoma to the bladder. The patient died of liver failure in March 2012.


Subject(s)
Bile Duct Neoplasms , Bile Ducts, Intrahepatic , Cholangiocarcinoma , Urinary Bladder Neoplasms , Adult , Aged, 80 and over , Bile Duct Neoplasms/pathology , Cholangiocarcinoma/secondary , Cholangiocarcinoma/surgery , Cholangiopancreatography, Endoscopic Retrograde , Humans , Male , Urinary Bladder , Urinary Bladder Neoplasms/secondary , Urinary Bladder Neoplasms/surgery
11.
Nihon Hinyokika Gakkai Zasshi ; 107(1): 48-53, 2016.
Article in Japanese | MEDLINE | ID: mdl-28132992

ABSTRACT

We report a 33-year-old male with a left advanced non-seminomatous testicular germ cell tumor (NSGCT) accompanied panic disorder. He had experienced palpitation and hyperpnea in crowds in his twenties. He was admitted to the Department of Otorhinolaryngology with the chief complaint of left neck swelling. 18F-fluorodeoxy glucose positron emission tomography/computed tomography (FDG-PET/CT) demonstrated left neck, left supraclavicular, left axillary, and paraaortic lymph node (LN) swelling and left testicular swelling. He was referred to our department. The left testis had enlarged to the size of a fist. He rejected admission at that time, but next day, he was taken to our hospital by an ambulance because he lost consciousness at home. No abnormalities were found in the brain CT and electrocardiogram. He was admitted and left high orchiectomy was performed. The human chorionic gonadotropin (HCG) level had elevated to 9,717 IU/L and alpha fetoprotein level (AFP) had elevated to 427 ng/ml. The histopathological diagnosis was tumors of more than one histological type, mixed forms: seminoma and embryonal carcinoma.He had palpitation and hyperpnea after admission and was diagnosed with panic disorder by a psychiatrist. Psychotropic drugs (fluvoxamine maleate 50 mg/day, alprazolam 0.8 mg/day) were prescribed and the panic attacks disappeared afterwards. The psychiatric social worker supported his mind side. Bleomycin, etoposide, and cisplatin (BEP) therapy was performed for 4 courses. He put on a blanket to his face and came to avoid a conversation with other people during the chemotherapy. He was diagnosed with depression and psychotropic drugs were increased (fluvoxamine maleate 50→75 mg/day, alprazolam 0.8→1.2 mg/day) in quantity.Lymphadenectomies for LN metastases were performed and their histopathological examination revealed the existence of viable embryonal carcinoma in the supraclavicular LN. Etoposide, ifosfamide, and cisplatin (VIP) therapy was performed for 2 courses.The pateint has remained alive without tumor recurrence. Psychotropic drugs were reduced and the recent drug is fluvoxamine maleate 25 mg/day.


Subject(s)
Carcinoma, Embryonal/complications , Carcinoma, Embryonal/therapy , Neoplasms, Germ Cell and Embryonal/complications , Neoplasms, Germ Cell and Embryonal/therapy , Neoplasms, Multiple Primary , Panic Disorder/complications , Testicular Neoplasms/complications , Testicular Neoplasms/therapy , Adult , Alprazolam/administration & dosage , Antineoplastic Combined Chemotherapy Protocols/therapeutic use , Biomarkers, Tumor/blood , Carcinoma, Embryonal/diagnosis , Chorionic Gonadotropin/blood , Combined Modality Therapy , Fluvoxamine/administration & dosage , Humans , Lymph Node Excision , Male , Neoplasms, Germ Cell and Embryonal/diagnosis , Orchiectomy , Panic Disorder/drug therapy , Positron Emission Tomography Computed Tomography , Psychotropic Drugs/administration & dosage , Testicular Neoplasms/diagnosis , Treatment Outcome , alpha-Fetoproteins
12.
Case Rep Obstet Gynecol ; 2014: 602139, 2014.
Article in English | MEDLINE | ID: mdl-24551466

ABSTRACT

Several etiologies have been proposed for erythrocytosis associated with uterine leiomyoma. We report a case of erythrocytosis associated with a large uterine leiomyoma, in which specific immunostaining for erythropoietin was positive. A 55-year-old woman, gravida 0, para 0, was referred to our hospital for treatment for a large uterine myoma and erythrocytosis. She had no vaginal bleeding after she reached menopause at 50 years old. She had severe polycythemia: hemoglobin (Hb), 19.9 g/dL; red blood cell count (RBC), 6.65 × 10(6)/mm(3); hematocrit, (Hct) 59.1%. An abdominal simple hysterectomy was performed, and a pathological examination confirmed the diagnosis of leiomyoma of the uterus. In addition, immunostaining demonstrated that the cytoplasm of the leiomyoma cells was strongly positive for erythropoietin. After the operation, the patient's hemoglobin and hematocrit levels normalized, and we diagnosed her condition as myomatous erythrocytosis syndrome.

13.
Hinyokika Kiyo ; 59(3): 179-81, 2013 Mar.
Article in Japanese | MEDLINE | ID: mdl-23633634

ABSTRACT

A 64-year-old woman presented to our hospital with the chief complaints of abdominal pain and appetite loss, and she was admitted to the internal medicine department. Kidney, ureter and bladder X-ray revealed intrapelvic calcification near the bladder, and so, the patient consulted our department. Computed tomography and magnetic resonance imaging revealed an urachal abscess accompanied by a stone. Open surgery was performed under general anesthesia. The mass adhered tightly to the intestine and bladder. The urachal abscess ruptured during the operation, and pus leaked into the intraabdominal cavity. Partial cystectomy was performed to remove the mass completely. The stone existed in the urachal abscess, and its constituents were CaOxa (51%) and CaP (49%). The pathological diagnosis was urachal abscess without malignancy.


Subject(s)
Abscess/diagnosis , Urachus , Urinary Calculi/complications , Abscess/surgery , Female , Humans , Middle Aged , Urinary Calculi/diagnosis , Urinary Calculi/surgery
14.
Nihon Hinyokika Gakkai Zasshi ; 104(6): 702-5, 2013 Nov.
Article in Japanese | MEDLINE | ID: mdl-24564077

ABSTRACT

We report a case of a 73-year-old male with heterochronous triple urogenital cancer. The patient was referred to our hospital because serum PSA was elevated (7.0 ng/ml) in 1998. Prostatic needle biopsy revealed prostatic cancer in the right lobe, and total prostatectomy was performed. The histopathological diagnosis was moderately differentiated adenocarcinoma (TlcNOMO). Non-muscle invasive bladder cancer (NMIBC) was detected during an examination for microhematuria in 2002. Transurethral resection of the bladder tumor (TURBT) procedure was performed, and the histopathological diagnosis was grade 2 urothelial carcinoma (pTa). A right renal mass was detected incidentally on follow-up CT for bladder cancer in 2008. Renal enucleation was performed in 2009. The histopathological diagnosis was grade 2 clear cell renal cell carcinoma (pTlaNXMO). NMIBC was detected on follow-up urethrocystoscopy in 2011. The TURBT procedure was performed, and the histopathological diagnosis was grade 2 urothelial carcinoma (pTa). On follow-up for urogenital cancer patients, it is important to investigate recurrence of the primary cancer and also heterochronous canceration of other urogenital organs.


Subject(s)
Adenocarcinoma/surgery , Carcinoma, Renal Cell/surgery , Carcinoma/surgery , Kidney Neoplasms/surgery , Neoplasms, Multiple Primary , Prostatic Neoplasms/surgery , Urinary Bladder Neoplasms/surgery , Adenocarcinoma/diagnosis , Adenocarcinoma/pathology , Aged , Carcinoma/diagnosis , Carcinoma/pathology , Carcinoma, Renal Cell/diagnosis , Carcinoma, Renal Cell/pathology , Follow-Up Studies , Humans , Kidney Neoplasms/diagnosis , Kidney Neoplasms/pathology , Male , Prostatic Neoplasms/diagnosis , Prostatic Neoplasms/pathology , Treatment Outcome , Urinary Bladder Neoplasms/diagnosis , Urinary Bladder Neoplasms/pathology
15.
Mod Pathol ; 25(7): 956-67, 2012 Jul.
Article in English | MEDLINE | ID: mdl-22481280

ABSTRACT

Progressively transformed germinal centers is a benign condition of unknown pathogenesis characterized by a distinctive variant form of reactive follicular hyperplasia in lymph nodes. We recently reported Ig G4-related disease in progressively transformed germinal centers. However, no large case series has been reported and clinicopathologic findings remain unclear. Here, we report 40 Japanese patients (28 men, 12 women; median age, 56 years) with progressively transformed germinal centers of the lymph nodes who fulfilled the histological diagnostic criteria for IgG4-related disease (IgG4(+) progressively transformed germinal centers), with asymptomatic localized lymphadenopathy involving the submandibular nodes in 24, submandibular and cervical nodes in 14, cervical nodes only in 1, and cervical and supraclavicular nodes in 1. In all, 16 (52%) of 31 examined patients had allergic disease. Histologically, the lymph nodes demonstrated uniform histological findings, namely marked follicular hyperplasia with progressively transformed germinal centers, and localization of the majority of IgG4(+) plasma cells in the germinal centers. Serum IgG4, serum IgE and peripheral blood eosinophils were elevated in 87%, 92% and 53% of examined patients, respectively. Eighteen patients subsequently developed extranodal lesions (including five who developed systemic disease), which on histological examination were consistent with IgG4-related disease. IgG4(+) progressively transformed germinal centers presents with uniform clinicopathological features of asymptomatic localized submandibular lymphadenopathy, which persists and/or relapses, and sometimes progresses to extranodal lesions or systemic disease. Nine patients were administered steroid therapy when the lesions progressed, to which all responded well. We suggest that IgG4(+) progressively transformed germinal centers should be included in the IgG4-related disease spectrum.


Subject(s)
Germinal Center/pathology , Immunoglobulin G , Lymphatic Diseases/pathology , Adult , Aged , Female , Humans , Immunohistochemistry , Male , Middle Aged
16.
Pathol Int ; 60(8): 566-74, 2010 Aug.
Article in English | MEDLINE | ID: mdl-20618734

ABSTRACT

Lymphohistiocytoid mesothelioma (LHM), reported to be a rare variant of sarcomatoid mesothelioma, is challenging to differentiate from non-Hodgkin's lymphoma due to marked lymphocytic infiltration. To aid accurate recognition of LHM, we examined immunohistochemical, in situ hybridization (ISH) of Epstein-Barr virus RNA (EBER-1) mRNA, fluorescence ISH (FISH) for homozygous deletion of 9p21, and asbestos analysis in four cases (three men and 1 woman). Three patients died, while Case 4 was still alive 19 months after extrapleural pneumonectomy. Histologically, these cases were characterized by heavy lymphocytic infiltration. All neoplastic cells were positive for calretinin, AE1/AE3, and epithelial membrane antigen, but negative for CEA. EBER1 factor was negative. FISH analysis demonstrated homozygous deletion of the 9p21 locus in three of the four cases. In Case 1: (i) autopsy findings showed mesothelioma primarily located in the right parietal pleura, but metastasized into the left lung and abdominal organs; (ii) the histological findings at autopsy indicated sarcomatoid mesothelioma; and (iii) we found asbestos bodies and fibers in extracts from lung tissue (Cases 1 & 4) using digestion with bleaching fluid. LHM, an infrequent variant of sarcomatoid mesothelioma, displayed homozygous deletion of the 9p21 locus (three of four cases), and has a relatively favorable prognosis for the sarcomatoid type.


Subject(s)
Mesothelioma/pathology , Pleural Neoplasms/pathology , Biomarkers, Tumor/genetics , Biomarkers, Tumor/metabolism , Female , Herpesvirus 4, Human/genetics , Herpesvirus 4, Human/metabolism , Humans , Immunohistochemistry , In Situ Hybridization , Male , Mesothelioma/genetics , Mesothelioma/metabolism , Microscopy, Electron , Middle Aged , Pleural Neoplasms/genetics , Pleural Neoplasms/metabolism , RNA, Viral/genetics , RNA, Viral/metabolism
17.
Nihon Kokyuki Gakkai Zasshi ; 48(12): 918-22, 2010 Dec.
Article in Japanese | MEDLINE | ID: mdl-21226298

ABSTRACT

A 78-year-old man with complaints of appetite loss and weight loss visited our hospital in November 2006. Positron-emission tomography and computed tomography (PET/CT) showed swollen lymph nodes in the abdominal para-aorta, mediastinum and neck, with intense FDG accumulation. The pathological findings of the cervical lymph nodes revealed small-cell cancer. We diagnosed extensive small-cell lung cancer (SCLC), which occurred primarily in the left upper lobe. As subsequent CT revealed spontaneous shrinkage of the pulmonary nodule and swollen lymph nodes, the clinical course was monitored without anticancer therapy. In February 2007, progressive muscle weakness of the lower extremities developed. In July he was admitted with respiratory failure and required mechanical ventilation. Although we did not administer anticancer therapy due to his poor performance status, he survived for 30 months receiving mechanical ventilation, and the tumors continued to grow moderately. We diagnosed Lambert-Eaton myasthenic syndrome (LEMS) based on the clinical symptoms, the presence of anti-VGCC antibodies and waxing phenomenon on electromyography obtained in April 2009. Chemotherapy with amrubicin shrank the tumors, but his muscle weakness did not improve. Previous reports showed that a prognosis of SCLC with LEMS was better than that without LEMS. In this case, the tumors showed spontaneous regression without any anticancer therapy, and then increased moderately. The immune response was considered to have affected tumor growth.


Subject(s)
Lambert-Eaton Myasthenic Syndrome/complications , Lung Neoplasms/complications , Small Cell Lung Carcinoma/complications , Aged , Anthracyclines/therapeutic use , Antineoplastic Agents/therapeutic use , Calcium Channels/immunology , Humans , Lambert-Eaton Myasthenic Syndrome/diagnosis , Lambert-Eaton Myasthenic Syndrome/immunology , Lung Neoplasms/diagnosis , Lung Neoplasms/immunology , Lung Neoplasms/therapy , Male , Respiration, Artificial , Respiratory Insufficiency/etiology , Respiratory Insufficiency/therapy , Small Cell Lung Carcinoma/diagnosis , Small Cell Lung Carcinoma/immunology , Small Cell Lung Carcinoma/therapy , Time Factors
18.
Drug Metab Dispos ; 35(10): 1832-9, 2007 Oct.
Article in English | MEDLINE | ID: mdl-17639025

ABSTRACT

Isoline, a major retronecine-type pyrrolizidine alkaloid (PA) from the Chinese medicinal herb Ligularia duciformis, was suggested to be the most toxic known PA. Its in vitro metabolism was thus examined in rat and mouse liver microsomes, and its toxicity was compared with that of clivorine and monocrotaline after i.p. injection in mice. Isoline was more rapidly metabolized by both microsomes than clivorine and monocrotaline and converted to two polar metabolites M1 and M2, which were spectroscopically determined to be bisline (a deacetylated metabolite of isoline) and bisline lactone, respectively. Both metabolites were formed in the presence or absence of an NADPH-generating system with liver microsomes but not cytosol. Their formation was completely inhibited by the esterase inhibitors, triorthocresyl phosphate (TOCP) and phenylmethylsulfonyl fluoride, but not at all or partially by cytochrome P450 (P450) inhibitors, alpha-naphthoflavone and proadifen (SKF 525A), respectively. These results demonstrated that both metabolites were produced by microsomal esterase(s) but not P450 isozymes. The esterase(s) involved showed not only quite different activities but also responses to different inhibitors in rat and mouse liver microsomes, suggesting that different key isozyme(s) or combinations might be responsible for the deacetylation of isoline. Isoline injected i.p. into mice induced liver-specific toxicity that was much greater than that with either clivorine or monocrotaline, as judged by histopathology as well as serum alanine aminotransferase and aspartate aminotransferase levels. Isoline-induced hepatotoxicity was remarkably enhanced by the esterase inhibitor TOCP but was reduced by the P450 inhibitor SKF 525A, indicating that rodent hepatic esterase(s) played a principal role in the detoxification of isoline via rapid deacetylation in vivo.


Subject(s)
Asteraceae/chemistry , Esterases/antagonists & inhibitors , Pyrrolizidine Alkaloids/metabolism , Pyrrolizidine Alkaloids/toxicity , Alanine Transaminase/blood , Animals , Antitussive Agents/metabolism , Antitussive Agents/toxicity , Aspartate Aminotransferases/blood , Benzoflavones/pharmacology , Cytochrome P-450 Enzyme Inhibitors , Drugs, Chinese Herbal/metabolism , Drugs, Chinese Herbal/toxicity , Esterases/metabolism , Expectorants/metabolism , Expectorants/toxicity , Liver/drug effects , Liver/pathology , Male , Mice , Mice, Inbred Strains , Microsomes, Liver/metabolism , Monocrotaline/metabolism , Monocrotaline/toxicity , Phenylmethylsulfonyl Fluoride/pharmacology , Proadifen/pharmacology , Rats , Rats, Sprague-Dawley , Tritolyl Phosphates/pharmacology
19.
Intern Med ; 46(14): 1123-6, 2007.
Article in English | MEDLINE | ID: mdl-17634712

ABSTRACT

A 74-year-old man was referred to our hospital because of hypertension, blue toe syndrome and an elevation of serum creatinine from 0.8 to 1.4 mg/dl for eleven months. He had no history of invasive vascular procedures. Atherosclerosis was initially suspected, but renal impairment was accelerated following anticoagulant therapy. A renal biopsy established the diagnosis of cholesterol crystal embolism. Withdrawal of anticoagulants and the combination therapy with LDL apheresis and corticosteroids led to stabilization of the renal function. In patients with risk factors for atherosclerosis, cholesterol crystal embolism should be included in the differential diagnosis of chronic kidney disease.


Subject(s)
Embolism, Cholesterol/diagnosis , Aged , Arteriosclerosis Obliterans/diagnosis , Chronic Disease , Creatinine/blood , Diagnosis, Differential , Embolism, Cholesterol/complications , Embolism, Cholesterol/therapy , Humans , Hypertension/diagnosis , Hypertension/etiology , Hypertension/therapy , Kidney Diseases/blood , Kidney Diseases/etiology , Kidney Diseases/pathology , Kidney Diseases/therapy , Male , Treatment Outcome
20.
Intern Med ; 45(15): 897-901, 2006.
Article in English | MEDLINE | ID: mdl-16946571

ABSTRACT

A 65-year-old man underwent transurethral resection of the prostate on a diagnosis of benign prostatic hypertrophy. Almost simultaneously, a diagnostic resection of minor salivary glands was performed. After the resections he suffered from obstructive jaundice. Laboratory examinations revealed an increase in eosinophils and an elevation of serum IgG4. Pancreaticoduodenectomy was performed because of the possibility of pancreatic cancer. The prostate, salivary glands and pancreas showed common histological characteristics, namely, infiltration of lymphocytes and plasma cells accompanying dense fibrosis. Most of the infiltrating plasma cells showed strong immunoreactivity to IgG4. This is the first case with IgG4-associated prostatitis complicating autoimmune pancreatitis.


Subject(s)
Autoimmune Diseases/complications , Immunoglobulin G/blood , Pancreatitis/complications , Prostatitis/complications , Aged , Autoimmune Diseases/blood , Autoimmune Diseases/diagnostic imaging , Humans , Male , Pancreatitis/blood , Pancreatitis/diagnostic imaging , Prostatitis/blood , Prostatitis/diagnostic imaging , Radiography
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