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1.
Appl Immunohistochem Mol Morphol ; 25(1): e1-e8, 2017 01.
Article in English | MEDLINE | ID: mdl-27093448

ABSTRACT

We report a case of Epstein-Barr virus (EBV)-associated T-cell lymphoma of gastrointestinal (GI) tract from a 70-year-old white woman who initially presented with a widespread GI inflammation and gastric obstruction. Initial biopsies of the GI tract showed severe chronic inflammation in the esophagus, stomach, and the small intestine. Celiac disease and inflammatory bowel disease were ruled out. The patient was treated with partial gastrectomy. Histology showed gastric wall thickening with EBV-positive, mixed lymphocytic and plasma cell infiltration in the mucosa, and thickening and fibrosis of the submucosa. She developed EBV-associated T-cell lymphoma of the GI tract one and a half years later and expired due to multiorgan failure. The T-cell lymphoma diffusely infiltrated the GI wall without forming a mass lesion. The lymphoma expressed EBV and cytotoxic molecules but lacked common features of extranodal natural killer/T-cell lymphoma nasal type, such as angioinvasion/angiodestruction, necrosis, or CD56 expression. Immunoglobulin heavy chain (IGH) gene and T-cell receptor-γ gene rearrangements and EBV-positive cells were detected at the early stage of the disease. While IGH clones were transient, T-cell clones and EBV-positive cells progressively increased over the disease course. We conclude that this case is best classified as EBV-associated peripheral T-cell lymphoma of GI tract. Age-related immune senescence may have contributed to the uncontrolled GI inflammation and subsequent transformation to T-cell lymphoma.


Subject(s)
Epstein-Barr Virus Infections/pathology , Inflammation/pathology , Lymphoma, T-Cell, Peripheral/pathology , Aged , Chronic Disease , Female , Humans , In Situ Hybridization , Lymphoma, T-Cell, Peripheral/virology
2.
Case Rep Pancreat Cancer ; 2(1): 46-49, 2016.
Article in English | MEDLINE | ID: mdl-30631815

ABSTRACT

Background: Acinar cell carcinoma is a rare form of pancreatic cancer, accounting for 1-2% of all cases of exocrine pancreatic neoplasms in adults. Due to its rarity, no randomized controlled trials have been performed to determine the optimal treatment options. As such, high-quality case reports and case series are needed to help guide clinicians in the management of this deadly disease. Case Presentation: A 56-year-old Caucasian male presenting with abdominal pain and weight loss was diagnosed with stage III acinar cell carcinoma of the pancreatic body with celiac axis involvement. Although initially deemed unresectable, the patient responded favorably to nine cycles of 5-fluorouracil-based neoadjuvant chemotherapy. The tumor was successfully resected through distal pancreatectomy with en bloc splenectomy and en bloc celiac artery resection (Appleby procedure). Final pathology analysis showed negative resection margins and complete chemotherapeutic response within the pancreas, with residual tumor cells detected in only a single peripancreatic lymph node. Conclusion: 5-fluorouracil-based chemotherapy may be a promising option for the neoadjuvant treatment of locally unresectable acinar cell carcinoma. With sufficient expertise, negative surgical resection margins are possible even with vascular involvement. Due to the generally poor prognosis associated with acinar cell carcinoma, such aggressive treatment measures are warranted.

3.
Case Rep Pancreat Cancer ; 1(1): 16-21, 2015.
Article in English | MEDLINE | ID: mdl-30631804

ABSTRACT

Background: Correct preoperative diagnosis of hepatobiliary disease can be challenging-even with current advances in radiographical imaging, laboratory testing, and endoscopic evaluation. Case presentation 1: A 65-year-old female with painless jaundice and weight loss was found to have cholelithiasis complicated by the Mirizzi syndrome. Case presentation 2: A 71-year-old female with new-onset painless jaundice and impacted stone in the gallbladder neck was found to have a cholangiocarcinoma. Case presentation 3: A 70-year-old male with progressive painless jaundice and weight loss was found to have a pancreatic adenocarcinoma. Conclusion: Proper diagnosis and management of patients with painless jaundice can be difficult in the preoperative setting and may require surgical exploration to obtain a definitive diagnosis.

4.
J Gastrointest Oncol ; 5(6): E96-9, 2014 Dec.
Article in English | MEDLINE | ID: mdl-25436139

ABSTRACT

Neurofibromatosis type 1 (NF-1) is an autosomal dominant genetic disorder with a known predisposition to gastrointestinal neoplasms such as stromal tumors and carcinoids. Adenocarcinomas (ACs) of the gastrointestinal tract are relatively rare in patients with NF-1, especially those found in the periampullary region. We present a case report of periampullary adenocarcinoma in a 56-year-old woman with NF-1 who presented with abdominal pain and obstructive jaundice.

5.
Open Forum Infect Dis ; 1(2): ofu087, 2014 Sep.
Article in English | MEDLINE | ID: mdl-25734153

ABSTRACT

Enteric anisakiasis is a known parasitic infection. To date, human infection has been reported as resulting from the inadvertent ingestion of the anisakis larvae when eating raw/undercooked fish, squid, or eel. We present a first reported case of intestinal obstruction caused by anisakiasis, after the ingestion of raw clams.

6.
Radiology ; 268(2): 581-8, 2013 Aug.
Article in English | MEDLINE | ID: mdl-23525208

ABSTRACT

PURPOSE: To compare subharmonic aided pressure estimation (SHAPE) with pressure catheter-based measurements in human patients with chronic liver disease undergoing transjugular liver biopsy. MATERIALS AND METHODS: This HIPAA-compliant study had U.S. Food and Drug Administration and institutional review board approval, and written informed consent was obtained from all participants. Forty-five patients completed this study between December 2010 and December 2011. A clinical ultrasonography (US) scanner was modified to obtain SHAPE data. After transjugular liver biopsy with pressure measurements as part of the standard of care, 45 patients received an infusion of a microbubble US contrast agent and saline. During infusion, SHAPE data were collected from a portal and hepatic vein and were compared with invasive measurements. Correlations between data sets were determined by using the Pearson correlation coefficient, and statistical significance between groups was determined by using the Student t test. RESULTS: The 45 study patients included 27 men and 18 women (age range, 19-71 years; average age, 55.8 years). The SHAPE gradient between the portal and hepatic veins was in good overall agreement with the hepatic venous pressure gradient (HVPG) (R = 0.82). Patients at increased risk for variceal hemorrhage (HVPG ≥ 12 mm Hg) had a significantly higher mean subharmonic gradient than patients with lower HVPGs (1.93 dB ± 0.61 [standard deviation] vs -1.47 dB ± 0.29, P < .001), with a sensitivity of 100% and a specificity of 81%, indicating that SHAPE may be a useful tool for the diagnosis of clinically important portal hypertension. CONCLUSION: Preliminary results show SHAPE to be an accurate noninvasive technique for estimating portal hypertension.


Subject(s)
Hepatic Veins , Hypertension, Portal/diagnostic imaging , Hypertension, Portal/physiopathology , Liver Cirrhosis/diagnostic imaging , Liver Cirrhosis/physiopathology , Adult , Aged , Biopsy , Chronic Disease , Contrast Media , Female , Ferric Compounds , Humans , Iron , Male , Middle Aged , Oxides , Pilot Projects , ROC Curve , Sensitivity and Specificity , Ultrasonography, Interventional
7.
AJR Am J Roentgenol ; 195(3): 661-8, 2010 Sep.
Article in English | MEDLINE | ID: mdl-20729444

ABSTRACT

OBJECTIVE: The objectives of this article are to review the radiologic, pathologic, and clinical features of diffuse idiopathic pulmonary neuroendocrine cell hyperplasia, tumorlet, and carcinoids and to discuss the possible role of diffuse idiopathic pulmonary neuroendocrine cell hyperplasia and tumorlet in the development of carcinoids. CONCLUSION: Given the potential significant morbidity of diffuse idiopathic pulmonary neuroendocrine cell hyperplasia and its neoplastic counterparts, it is important to understand and recognize these disease entities. A conceptual continuum of these neuroendocrine entities is suggested.


Subject(s)
Carcinoid Tumor/pathology , Lung Neoplasms/pathology , Neuroendocrine Cells/pathology , Neuroendocrine Tumors/pathology , Carcinoid Tumor/diagnostic imaging , Cell Proliferation , Contrast Media , Diagnosis, Differential , Humans , Lung Neoplasms/diagnostic imaging , Neuroendocrine Tumors/diagnostic imaging , Neurosecretory Systems/pathology , Precancerous Conditions/diagnostic imaging , Precancerous Conditions/pathology , Risk Factors , Tomography, X-Ray Computed
8.
Blood ; 109(7): 3099-107, 2007 Apr 01.
Article in English | MEDLINE | ID: mdl-17119123

ABSTRACT

Well-characterized mouse models of allo-immune antibody-mediated hemolysis would provide a valuable approach for gaining greater insight into the pathophysiology of hemolytic transfusion reactions. To this end, mouse red blood cells (mRBCs) from human glycophorin A transgenic (hGPA-Tg) donor mice were transfused into non-Tg recipients that had been passively immunized with IgG or IgM hGPA-specific monoclonal antibodies (mAbs). In this novel murine "blood group system," mRBCs from hGPA-Tg mice are "antigen positive" and mRBCs from non-Tg mice are "antigen negative." Passive immunization of non-Tg mice with the IgG1 10F7 and IgG3 NaM10-2H12 anti-hGPA mAbs each induced rapid clearance of incompatible transfused hGPA-Tg-mRBCs in a dose-response manner. Using various knockout mice as transfusion recipients, both the complement system and activating Fcgamma receptors were found to be important in the clearance of incompatible mRBCs by each of these IgG mAbs. In addition, the IgM E4 anti-hGPA mAb induced complement-dependent intravascular hemolysis of transfused incompatible hGPA-Tg-mRBCs accompanied by gross hemoglobinuria. These initial studies validate the relevance of these new mouse models for addressing important questions in the field of transfusion medicine.


Subject(s)
Hemolysis/immunology , Immunoglobulin G/blood , Immunoglobulin M/blood , Transfusion Reaction , Animals , Antibodies, Monoclonal , Complement System Proteins/metabolism , Disease Models, Animal , Glycophorins/genetics , Humans , Immunization, Passive , In Vitro Techniques , Isoantibodies/blood , Mice , Mice, Inbred BALB C , Mice, Inbred C57BL , Mice, Knockout , Mice, Transgenic , Receptors, IgG/blood
9.
Am J Clin Pathol ; 120 Suppl: S14-24, 2003 Dec.
Article in English | MEDLINE | ID: mdl-15298140

ABSTRACT

Since the introduction of the triple screen, the emergence of additional analytes found to be associated with trisomy 21 pregnancies has challenged the clinical pathology and obstetric communities to determine which combination provides the best performance characteristics as a screening test. The cost, practicality, and psychosocial and ethical dimensions of different screening regimens further complicate the issue. This review attempts to give an overview of the various markers, current methods of screening, and most promising recent developments in antenatal screening for Down syndrome, with an emphasis on performance in prospective studies that have emerged during the last few years, rather than on estimates from statistical modeling.


Subject(s)
Down Syndrome/diagnosis , Prenatal Diagnosis/methods , Chorionic Gonadotropin/blood , Cost-Benefit Analysis , Estriol/blood , Female , Humans , Pregnancy , Pregnancy Trimester, First , Pregnancy-Associated Plasma Protein-A/analysis , alpha-Fetoproteins/analysis
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