Research Topics
| Susan C AbrahamSummaryAffiliation: Johns Hopkins University Country: USA Publications
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Publications
Paget cells in the esophagus: assessment of their histopathologic features and near-universal association with underlying esophageal adenocarcinomaSusan C Abraham
Department of Pathology, M D Anderson Cancer Center, Houston, TX, USA
Am J Surg Pathol 32:1068-74. 2008..A commonality among cases with Paget cells is the presence of focal or diffuse, poorly differentiated adenocarcinoma with discohesive cells. E-cadherin alterations seem to play a less significant role...
Gastric adenomas: intestinal-type and gastric-type adenomas differ in the risk of adenocarcinoma and presence of background mucosal pathologySusan C Abraham
Divison of Gastrointerstinal Liver Pathology, Department of Pahology, Johns Hopkins University School of Medicine, Baltimeore, Maryland
Am J Surg Pathol 26:1276-85. 2002..In any individual patient complete removal of the adenoma should be performed, and thorough biopsy of the surrounding gastric mucosa is essential to understand the clinicopathologic context of the adenoma...
Solid-pseudopapillary tumors of the pancreas are genetically distinct from pancreatic ductal adenocarcinomas and almost always harbor beta-catenin mutationsSusan C Abraham
Department of Pathology, Division of Gastrointestinal Liver Pathology, The Johns Hopkins University School of Medicine, Baltimore, Maryland 21205 2196, USA
Am J Pathol 160:1361-9. 2002..Overexpression of p53 was limited to only 3 of 19 (15.8%) SPTs. These results emphasize the two distinct, divergent genetic pathways of neoplastic progression in pancreatic ductal and nonductal neoplasms...
Frequent CpG island methylation in precursor lesions and early gastric adenocarcinomasJae-Hyuk Lee
Department of Pathology, MD Anderson Cancer Center, Houston, TX 77030, USA
Oncogene 23:4646-54. 2004..Methylation of the p16 gene may contribute to the malignant transformation of gastric precursor lesions...
Genetic alterations in gastric adenomas of intestinal and foveolar phenotypesSusan C Abraham
Department of Pathology, Mayo Clinic, Rochester, MN 55905, USA
Mod Pathol 16:786-95. 2003..Although intestinal-type and foveolar-type gastric adenomas display divergent biologic behavior, the specific genetic events accounting for these differences in morphology and biologic behavior are unclear...
Hepatic adenomas: analysis of sex steroid receptor status and the Wnt signaling pathwayMichael Torbenson
Division of Gastrointestinal Liver Pathology, Department of Pathology, The Johns Hopkins University School of Medicine, Baltimore, Maryland 21205 2196, USA
Mod Pathol 15:189-96. 2002..Activation of the Wnt signaling pathway appears to be important in a subset of hepatic adenomas but does not result from common beta-catenin or APC mutations and does not appear to be directly linked to hormonal receptor status...
Genetic and immunohistochemical analysis of pancreatic acinar cell carcinoma: frequent allelic loss on chromosome 11p and alterations in the APC/beta-catenin pathwaySusan C Abraham
Department of Pathology, Division of GI LiverPathology, The Johns Hopkins University School of Medicine, Baltimore, Maryland 21205 2196, USA
Am J Pathol 160:953-62. 2002..These results indicate that ACCs are genetically distinct from pancreatic ductal adenocarcinomas, but some cases contain genetic alterations common to histologically similar pancreatoblastomas...
Significance of central perivenulitis in pediatric liver transplantationSusan C Abraham
Department of Pathology, M D Anderson Cancer Center, Houston, TX, USA
Am J Surg Pathol 32:1479-88. 2008..CP is most common in conjunction with portal ACR, where it carries a significant risk for the development of zone 3 fibrosis and a trend toward the development of ductopenic chronic rejection...
Molecular and immunohistochemical analysis of intraductal papillary neoplasms of the biliary tractSusan C Abraham
Department of Pathology, Mayo Clinic, Rochester, MN 55905, USA
Hum Pathol 34:902-10. 2003..Finally, the frequency of allelic loss on 18q suggests that a locus on 18q is involved in the molecular pathogenesis of biliary IPNs, but this locus is not DPC4...
Frequent CpG island methylation in sporadic and syndromic gastric fundic gland polypsSusan C Abraham
Department of Pathology, Mayo Clinic, Rochester, MN 55905, USA
Am J Clin Pathol 122:740-6. 2004..87). Epigenetic alterations involving methylation of CpG islands might have a role in the development of some FGPs, particularly those with a PPI effect. They do not account for the presence or absence of a dysplastic phenotype in FGPs...
Inverse relationship between APC gene mutation in gastric adenomas and development of adenocarcinomaJae Hyuk Lee
Department of Pathology, MD Anderson Cancer Center, Houston, Texas 77030, USA
Am J Pathol 161:611-8. 2002..Gastric adenomas or dysplasias without APC mutations but with or without MSI may have a different biological behavior, and are precursors of intestinal-type of gastric adenocarcinomas...
Duplicated muscularis mucosae invasion has similar risk of lymph node metastasis and recurrence-free survival as intramucosal esophageal adenocarcinomaJeannelyn S Estrella
Department of Pathology, The University of Texas MD Anderson Cancer Center, Houston, USA
Am J Surg Pathol 35:1045-53. 2011..EAC invasion into the space between duplicated MM confers a similar risk of lymph node metastasis and recurrence as those of intramucosal EAC, and LVI is the best predictor of lymph node status and RFS in pT1 EAC...
Results of pancreaticoduodenectomy for lymphoplasmacytic sclerosing pancreatitisJeffrey M Hardacre
Department of Surgery, The Johns Hopkins Hospital, 600 N. Wolfe Street, Baltimore, MD 21287-4688, USA
Ann Surg 237:853-8; discussion 858-9. 2003..Nevertheless, differentiation from pancreatic neoplasia remains difficult. Patients undergoing pancreaticoduodenectomy for LPSP have durable relief of symptoms and a subjectively improved quality of life...
Diffuse lymphoplasmacytic chronic cholecystitis is highly specific for extrahepatic biliary tract disease but does not distinguish between primary and secondary sclerosing cholangiopathySusan C Abraham
Department of Pathology, Hilton 11 Mayo Clinic, 220 First Street SW, Rochester, MN, USA
Am J Surg Pathol 27:1313-20. 2003..These results suggest that a pattern of diffuse lymphoplasmacytic chronic cholecystitis is highly specific for extrahepatic biliary tract disease but does not distinguish between primary and secondary cholangiopathies...
Analysis of novel tumor markers in pancreatic and biliary carcinomas using tissue microarraysSharon L Swierczynski
Department of Pathology, The Johns Hopkinds University School of Medicine, Baltimore, MD 21231, USA
Hum Pathol 35:357-66. 2004..Therefore, these markers are potentially useful in developing diagnostic tests and treatment paradigms for tumors involving the biliary system...
Lymphoplasmacytic chronic cholecystitis and biliary tract disease in patients with lymphoplasmacytic sclerosing pancreatitisSusan C Abraham
Department of Pathology, Hilton 11, Mayo Clinic, 200 First Street SW, Rochester, MN 55905, USA
Am J Surg Pathol 27:441-51. 2003....
Sporadic fundic gland polyps with epithelial dysplasia : evidence for preferential targeting for mutations in the adenomatous polyposis coli geneSusan C Abraham
Department of Pathology, Division of Gastrointestinal/Liver Pathology, The Johns Hopkins University School of Medicine, Baltimore, Maryland, USA
Am J Pathol 161:1735-42. 2002..The lack of microsatellite instability in FGPs in this study and of K-ras mutations in a previous study suggests that secondary genetic alterations are rare in both dysplastic and nondysplastic FGPs...
Precancerous bile duct pathology in end-stage primary sclerosing cholangitis, with and without cholangiocarcinomaJason T Lewis
Division of Anatomic Pathology, Department of Pathology, DeKalb Medical Center, Decatur, GA 30033, USA
Am J Surg Pathol 34:27-34. 2010..Dysplasia, however, is generally confined to large and septal-size bile ducts and its presence may not be recognized unless multiple sections specifically targeted to the biliary tree are examined...
Patchy distribution of pathologic abnormalities in autoimmune pancreatitis: implications for preoperative diagnosisVishal S Chandan
Department of Pathology, Division of Anatomic Pathology, Mayo Clinic, Rochester, MN 55905, USA
Am J Surg Pathol 32:1762-9. 2008..IgG4 immunostaining of apparently negative biopsies may be helpful, but only in a small minority of cases...
Pyloric gland adenoma: an entity distinct from gastric foveolar type adenomaZong Ming Chen
Department of Pathology, Johns Hopkins University, Baltimore, MD 21231 2410, USA
Am J Surg Pathol 33:186-93. 2009..Despite its bland histologic appearance, it is much more likely to be accompanied by background IM and autoimmune gastritis and can evolve into invasive adenocarcinoma displaying pyloric gland differentiation...
Sporadic fundic gland polyposis: a clinical, histological, and molecular analysisMichael Torbenson
Department of Pathology, The Johns Hopkins Hospital, Baltimore, Maryland, USA
Mod Pathol 15:718-23. 2002..The fundic gland polyps were histologically and genetically identical to single sporadic fundic gland polyps and demonstrated frequent somatic activating mutations in exon 3 of the beta-catenin gene...
"Seedling" mesenchymal tumors (gastrointestinal stromal tumors and leiomyomas) are common incidental tumors of the esophagogastric junctionSusan C Abraham
Division of Anatomic Pathology, Department of Pathology, Mayo Clinic, Rochester, MN 55905, USA
Am J Surg Pathol 31:1629-35. 2007..The common occurrence of microscopic GISTs compared with the rarity of clinically manifest and malignant esophagogastric GISTs suggests that additional genetic or epigenetic alterations must happen for neoplastic progression...
Tumor suppressor gene hypermethylation as a predictor of gastric stromal tumor behaviorMichael G House
Department of Surgery, The Johns Hopkins Medical Institutions, Baltimore, MD 21231 1000, USA
J Gastrointest Surg 7:1004-14; discussion 1014. 2003..This study supports the methylation status of E-cadherin as a prognostic marker for early GIST recurrence and survival...
Microsatellite instability in intraductal papillary neoplasms of the biliary tractSusan C Abraham
Division of Gastrointestinal Liver Pathology, Department of Pathology, The Johns Hopkins University School of Medicine, Baltimore, Maryland, USA
Mod Pathol 15:1309-17. 2002....
Mucosal colonization by metastatic carcinoma in the gastrointestinal tract: a potential mimic of primary neoplasiaJeannelyn S Estrella
Department of Pathology, The University of Texas M D Anderson Cancer Center, Houston, TX, USA
Am J Surg Pathol 35:563-72. 2011..In situ growth and presence of an apparent adenoma cannot be taken as prima facie evidence of a primary neoplasm...
CD44 loss in gastric stromal tumors as a prognostic markerElizabeth Montgomery
Johns Hopkins Medical Institutions, Baltimore, MD, USA
Am J Surg Pathol 28:168-77. 2004..Thus, the prognostic value of CD44s and isoform expression in GIST were evaluated by immunohistochemistry of tissue microarrays...
Excellent interobserver agreement on grading the extent of residual carcinoma after preoperative chemoradiation in esophageal and esophagogastric junction carcinoma: a reliable predictor for patient outcomeTsung Teh Wu
Department of Pathology, University of Texas M D Anderson Cancer Center, 1515 Holcombe Boulevard, Houston, TX 77030, USA
Am J Surg Pathol 31:58-64. 2007..The extent of residual carcinoma is a reliable and reproducible predictor of survival; this grading system may allow a novel and early means of comparing outcomes after different neoadjuvant treatment regimens...
Expression of melanoma antigens in epithelioid gastrointestinal stromal tumors: a potential diagnostic pitfallMehmet L Guler
Department of Pathology, Johns Hopkins University, Baltimore, MD 21231, USA
Arch Pathol Lab Med 132:1302-6. 2008..Most gastric gastrointestinal stromal tumors (GISTs) express CD117/c-kit, as do a subset of metastatic melanomas, leading to a diagnostic dilemma in some cases...
The prevalence and natural history of untreated isolated central perivenulitis in adult allograft liversAlyssa M Krasinskas
Department of Pathology, University of Pittsburgh, Pittsburgh, PA 15213 2546, USA
Liver Transpl 14:625-32. 2008..In summary, "transplant-associated" isolated CP occurs in 28% of adult patients, early CP is predictive of late CP, and late CP (often present as isolated CP) is associated with long-term liver injury in some patients...
Histologic abnormalities are common in protocol liver allograft biopsies from patients with normal liver function testsSusan C Abraham
Department of Pathology, M D Anderson Cancer Center, Houston, TX, USA
Am J Surg Pathol 32:965-73. 2008....
Eosinophilic pancreatitis and increased eosinophils in the pancreasSusan C Abraham
Department of Pathology, Hilton 11, Mayo Clinic, 220 First Street SW, Rochester, MN 55905, USA
Am J Surg Pathol 27:334-42. 2003..True eosinophilic pancreatitis, although a fascinating clinicopathologic entity, is one of the rarest causes of pancreatic eosinophilia...
Pancreaticoduodenectomy (Whipple resections) in patients without malignancy: are they all 'chronic pancreatitis'?Susan C Abraham
Department of Pathology, Mayo Clinic, Rochester, Minnesota, 55905, USA
Am J Surg Pathol 27:110-20. 2003..2%) and reveal a diverse group of clinicopathologically distinctive pancreatic and biliary tract disease...
Epidermal growth factor receptor, p53 mutation, and pathological response predict survival in patients with locally advanced esophageal cancer treated with preoperative chemoradiotherapyMichael K Gibson
Division of Medical Oncology, The Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins, Baltimore, Maryland 21231, USA
Clin Cancer Res 9:6461-8. 2003..This study evaluates the role of clinical and cellular markers in predicting CR and OS in patients with esophageal cancer...
Metastatic neuroendocrine tumour in the breast: a potential mimic of in-situ and invasive mammary carcinomaKyle D Perry
Division of Anatomic Pathology, Department of Pathology, Mayo Clinic, Rochester, MN, USA
Histopathology 59:619-30. 2011....
Colchicine effect in a colonic hyperplastic polyp. A lesion mimicking serrated adenomaMichael Torbenson
Division of Gastrointestinal/Liver Pathology, Department of Pathology, The Johns Hopkins University School of Medicine, Baltimore, MD 21205-2196, USA
Arch Pathol Lab Med 126:615-7. 2002..Distinguishing between hyperplastic polyp and serrated adenoma is important because of the different management implications and the increased potential for neoplastic progression in the latter...
Oxyntic mucosa pseudopolyps: a presentation of atrophic autoimmune gastritisAlyssa M Krasinskas
Department of Pathology, University of Pennsylvania Medical Center, Philadelphia, USA
Am J Surg Pathol 27:236-41. 2003..Although a limited number of previous studies have suggested this type of polypoid presentation may represent "early" atrophic gastritis, its persistence in three of our patients argues against this hypothesis...
Beta-catenin immunohistochemistry separates mesenteric fibromatosis from gastrointestinal stromal tumor and sclerosing mesenteritisElizabeth Montgomery
Department of Pathology, Johns Hopkins School of Medicine, Baltimore, Maryland 21205, USA
Am J Surg Pathol 26:1296-301. 2002..beta-Catenin staining identifies lesions that are, instead, mesenteric fibromatoses...
Atrophic autoimmune pangastritis: A distinctive form of antral and fundic gastritis associated with systemic autoimmune diseaseDragan Jevremovic
Department of Pathology, Mayo Clinic, Rochester, MN 55905, USA
Am J Surg Pathol 30:1412-9. 2006..The development of multifocal low-grade dysplasia in 1 patient, a 19-year-old woman, suggests that this condition might have neoplastic potential...
Bile duct dysplasia in the setting of chronic hepatitis C and alcohol cirrhosisMichael Torbenson
Department of Pathology, Johns Hopkins University School of Medicine, Baltimore, MD 21231, USA
Am J Surg Pathol 31:1410-3. 2007..Alcohol also seems to be a risk factor. The dysplastic changes are multifocal, involve septal sized bile ducts, and are typically papillary...
Fibromatosis of the breast and mutations involving the APC/beta-catenin pathwaySusan C Abraham
Department of Pathology, The Johns Hopkins University School of Medicine, Baltimore, MD 21205-2196, USA
Hum Pathol 33:39-46. 2002..The spectrum of beta-catenin and APC alterations is similar to that described for desmoid tumors of the abdomen, paraspinal region, and extremities...
Colonic spirochetosis in children and adultsAyman Koteish
Department of Medicine, Johns Hopkins University School of Medicine, Baltimore, MD, USA
Am J Clin Pathol 120:828-32. 2003..While treatment information remains limited, treatment can lead to resolution of symptoms in some cases...
Glycogen pseudoground glass change in hepatocytesJoshua Wisell
Department of Pathology, The Johns Hopkins Hospital, Baltimore, MD 21231, USA
Am J Surg Pathol 30:1085-90. 2006..The changes are generally seen in the background of mild chronic hepatitis with mild or no fibrosis. Glycogen pseudoground glass change can resolve, but may also persist for years...
Rosai-Dorfman disease confined to the breastJerzy J Morkowski
Department of Pathology, The University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA
Ann Diagn Pathol 14:81-7. 2010....
Autoimmune gastritis: distinct histological and immunohistochemical findings before complete loss of oxyntic glandsMichael Torbenson
Division of Gastrointestinal/Liver Pathology, Department of Pathology, The Johns Hopkins University School of Medicine, Baltimore, Maryland, USA
Mod Pathol 15:102-9. 2002....
Giant fibrovascular polyp of the esophagus. A lesion causing upper airway obstruction and syncopeMatthew R Fries
Department of Pathology, The Johns Hopkins University School of Medicine, Baltimore, MD, USA
Arch Pathol Lab Med 127:485-7. 2003..Despite their large size, giant fibrovascular polyps should be recognized radiologically and pathologically as benign lesions. However, they can result in significant morbidity...
Remission of severe autoimmune enteropathy after treatment with high-dose cyclophosphamideMaria M Oliva-Hemker
Department of Pediatrics, The Johns Hopkins University School of Medicine, Baltimore, Maryland 21187-2631, USA
J Pediatr Gastroenterol Nutr 36:639-43. 2003
The effect of the metabolic syndrome, hepatic steatosis and steatohepatitis on liver fibrosis in hereditary hemochromatosisLeon A Adams
Department of Gastroenterology and Hepatology, Mayo Clinic College of Medicine, Rochester, MI, USA
Liver Int 26:298-304. 2006..We sought to examine whether the metabolic syndrome, hepatic steatosis or steatohepatitis influenced hepatic fibrosis among patients with HH and iron overload...
Muscularis mucosae duplication and the musculo-fibrous anomaly in endoscopic mucosal resections for barrett esophagus: implications for staging of adenocarcinomaJason T Lewis
Division of Anatomic Pathology, Mayo Clinic, Rochester, MN 55905, USA
Am J Surg Pathol 32:566-71. 2008....
Duplication of the muscularis mucosae in Barrett esophagus: an underrecognized feature and its implication for staging of adenocarcinomaSusan C Abraham
Division of Anatomic Pathology, Mayo Clinic, Rochester, MN, USA
Am J Surg Pathol 31:1719-25. 2007..The 17% rate of angiolymphatic invasion and 10% rate of lymph node metastases in our patients with invasion into duplicated MM suggest that these tumors can behave aggressively despite their technically intramucosal location...
Adult autoimmune enteropathy: Mayo Clinic Rochester experienceSalma Akram
Division of Gastroenterology and Hepatology, Department of Internal Medicine, Mayo Clinic, Rochester, Minnesota, USA
Clin Gastroenterol Hepatol 5:1282-90; quiz 1245. 2007..Autoimmune enteropathy is a rare cause of intractable diarrhea associated with circulating gut autoantibodies and a predisposition to autoimmunity. It is rarely observed in adults, with only 11 cases reported to date...
Prevalence and risk factors for gallbladder neoplasia in patients with primary sclerosing cholangitis: evidence for a metaplasia-dysplasia-carcinoma sequenceJason T Lewis
Division of Anatomic Pathology, Mayo Clinic, Rochester, MN 55905, USA
Am J Surg Pathol 31:907-13. 2007..The strong correlation between gallbladder dysplasia/adenocarcinoma and bile duct dysplasia/CC supports the concept of a neoplastic "field effect" along the intrahepatic and extrahepatic biliary tract in PSC...
Achlorhydria, parietal cell hyperplasia, and multiple gastric carcinoids: a new disorderSusan C Abraham
Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN 55905, USA
Am J Surg Pathol 29:969-75. 2005....
Surgical and chemotherapy treatment outcomes of goblet cell carcinoid: a tertiary cancer center experienceTuan H Pham
Department of Colorectal Surgery, Mayo Clinic, 200 First Street S.W, Rochester, Minnesota 55905, USA
Ann Surg Oncol 13:370-6. 2006..Surgical debulking is a consideration but is controversial. Adjuvant chemotherapy with 5-fluorouracil and leucovorin regimen is minimally effective against GCC...
Clinicopathologic findings and outcomes of liver transplantation using grafts from donors with unrecognized and unusual diseasesSurakit Pungpapong
Division of Gastroenterology and Hepatology, Mayo Clinic College of Medicine, Jacksonville, FL 32224, USA
Liver Transpl 12:310-5. 2006..In conclusion, long-term follow-up is necessary to confirm these findings and understand the impact of using these grafts...
Hemobilia caused by cytomegalovirus cholangiopathyGanapathy A Prasad
Division of Gastroenterology and Hepatology, Department of Medicine, Mayo Clinic College of Medicine, Rochester, Minnesota 55901, USA
Am J Gastroenterol 100:2592-5. 2005..Biliary CMV disease is rare in HIV-negative persons, but should be considered in a patient with unexplained hemobilia. Cholangioscopy may be useful for diagnosis...
Multicenter experience with upper gastrointestinal polyps in pediatric patients with familial adenomatous polyposisThomas M Attard
Department of Pediatrics, The University of Nebraska Medical Center, Omaha, NE 68198-5160, USA
Am J Gastroenterol 99:681-6. 2004..Patients with APC mutation between codon 1225-1694 may be more susceptible to aggressive gastroduodenal involvement in FAP...
Liver transplantation for severe intrahepatic noncirrhotic portal hypertensionAlyssa M Krasinskas
Departments of Pathology, University of Pittsburgh, PA, USA
Liver Transpl 11:627-34; discussion 610-1. 2005..Importantly, however, a diagnosis of cirrhosis is not required in this group of patients to qualify them for OLT, and these patients have good long-term graft function after OLT...
Distinguishing gastrointestinal stromal tumors from their mimics: an updateSusan C Abraham
Division of Anatomic Pathology, Mayo Clinic, Rochester, MN 55905, USA
Adv Anat Pathol 14:178-88. 2007..It is important to separate GISTs from these potential mimics because their treatment and prognosis can differ markedly...
Achlorhydria, parietal cell hyperplasia, and multiple gastric carcinoids: a new disorderPedram Argani
Am J Surg Pathol 31:488. 2007
Gastrointestinal plasmacytoma that caused anemia in a patient with multiple myelomaTuba Esfandyari
Mayo Clinic, Rochester, MN 55905, USA
Nat Clin Pract Gastroenterol Hepatol 4:111-5. 2007..He had required more than 15 U of packed red blood cells within a 2-month period for his anemia, despite recombinant erythropoietin treatment, and his hemoglobin level was persistently below 9 g/dl...
An assessment of chromosomal alterations detected by fluorescence in situ hybridization and p16 expression in sporadic and primary sclerosing cholangitis-associated cholangiocarcinomasRyan D DeHaan
Department of Laboratory Medicine and Pathology, Mayo Clinic College of Medicine, Rochester, MN 55905, USA
Hum Pathol 38:491-9. 2007..Polysomy and homozygous 9p21 deletion are common in both sporadic and PSC-associated CCAs and are frequently detectable in PSC-associated biliary dysplasia...
Chronic antral ulcer associated with gastroduodenal lymphocytic phlebitisSusan C Abraham
Department of Pathology and Laboratory Medicine, Mayo Clinic, Rochester, MN 55905, USA
Am J Surg Pathol 28:1659-63. 2004..We hypothesize that there may be more cases of upper gastrointestinal ELP than are diagnosed as such, in part because the diagnosis can be made only on surgical resections specimens...
