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1.
Hum Pathol ; 43(8): 1258-64, 2012 Aug.
Article in English | MEDLINE | ID: mdl-22305240

ABSTRACT

The relationship between higher total lymph node resection number in colorectal cancer resection specimens and improved overall survival is well known. Recent studies describe an association between a high rate of microsatellite instability and a high total lymph node count in colorectal cancer. Higher lymph node retrieval may potentially explain the improved survival seen in cancers with microsatellite instability. We investigate whether these associations can be validated in a cohort of American Joint Committee on Cancer stage III colon cancers. Medical records from 200 cases of stage III colon cancer resection specimens were reviewed, and sufficient tissue was available for 168. Expression of DNA mismatch repair proteins was determined by immunohistochemistry, and microsatellite status, by polymerase chain reaction. The mean total lymph node count in cases with microsatellite instability versus microsatellite stable tumors (15.9 versus 16.9; P = .664) and the mean number of negative lymph nodes in each respective category (12.2 versus 13.6; P = .522) were not significantly different. There was no difference between microsatellite stable cases and cases with microsatellite instability when total lymph node counts (P = .953) or negative lymph node counts (P = .381) were analyzed with respect to percentage of cases above and below the medians. This cohort of stage III colon cancers does not support a significant relationship between microsatellite status and a higher retrieval of total or negative lymph nodes. Although microsatellite instability is associated with improved overall survival in our cohort (P = .026), the reason for this does not appear to be related to higher numbers of retrieved lymph nodes.


Subject(s)
Colonic Neoplasms/genetics , Lymph Nodes/pathology , Lymphatic Metastasis/genetics , Microsatellite Instability , Adult , Aged , Aged, 80 and over , Colonic Neoplasms/pathology , Colonic Neoplasms/surgery , DNA Mismatch Repair , Female , Humans , Lymph Nodes/surgery , Lymphatic Metastasis/pathology , Male , Middle Aged , Neoplasm Staging
2.
J Cutan Pathol ; 38(12): 979-83, 2011 Dec.
Article in English | MEDLINE | ID: mdl-21899591

ABSTRACT

The persistent pigmented purpuric dermatitides (PPPD) are a spectrum of dermatologic disorders characterized by petechial and pigmented macules usually confined to the lower limbs. Their etiology is unknown and several clinical variants are recognized. At the microscopic level they are characterized by angiocentric lymphocytic inflammation, red blood cell extravasation and hemosiderin deposition. A granulomatous variant of the PPPD has recently been described and to date eleven cases have been reported in the literature. In contrast to the conventional type, this variant is characterized histopathologically by ill-defined, non-necrotizing granulomata admixed with the lymphocytic inflammatory background. Although initially the granulomatous variant of the PPPD was thought to occur only in Asian patients, this sole racial predilection has not been substantiated. A tenuous association with hyperlipidemia has been noted but this requires further study. The principal importance of recognizing this entity lies in the need to include it in the histopathological differential diagnosis of granulomatous dermal infiltrates. We report here an additional patient with the granulomatous variant of PPPD and elaborate on this entity in the context of existing information in the literature.


Subject(s)
Dermatitis/metabolism , Dermatitis/pathology , Purpura/metabolism , Purpura/pathology , Skin Pigmentation , Female , Hemosiderin/metabolism , Humans , Lymphocytes/pathology , Middle Aged
3.
Nature ; 419(6904): 270, 2002 Sep 19.
Article in English | MEDLINE | ID: mdl-12239559

ABSTRACT

Spliceosomal introns, one of the hallmarks of eukaryotic genomes, were thought to have originated late in evolution and were assumed not to exist in eukaryotes that diverged early -- until the discovery of a single intron with an aberrant splice boundary in the primitive 'protozoan' Giardia. Here we describe introns from a close relative of Giardia, Carpediemonas membranifera, that have boundary sequences of the normal eukaryotic type, indicating that canonical introns are likely to have arisen very early in eukaryotic evolution.


Subject(s)
Eukaryotic Cells/classification , Eukaryotic Cells/metabolism , Evolution, Molecular , Introns/genetics , Phosphotransferases (Carboxyl Group Acceptor)/genetics , Phylogeny , Animals , Base Sequence , Giardia/genetics , HSP70 Heat-Shock Proteins/genetics , RNA Splice Sites/genetics , RNA Splicing/genetics , RNA, Messenger/genetics , RNA, Messenger/metabolism , Reverse Transcriptase Polymerase Chain Reaction
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