Ultrastructural study of the pancreas in AIDS

被引:6
作者
Chehter, EZ
Duarte, MIS
Takakura, CFH
Longo, MA
Laudanna, AA
机构
[1] Univ Sao Paulo, Fac Med, Dept Gastroenterol,Sch Med, Disciplina Gastroenterol,Clin Gastroenterol Div, BR-01421000 Sao Paulo, Brazil
[2] Univ Sao Paulo, Sch Med, Dept Pathol, Lab Pathol Transmissable Dis, BR-01421000 Sao Paulo, Brazil
关键词
pancreas; transmission electron microscopy; ultrastructure; acinar organelles; HIV infection; malnutrition;
D O I
10.1097/00006676-200303000-00011
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Introduction: Frequent histologic changes (90%) in the pancreas suggesting protein-energy malnutrition were found in a previous necropsy study of pancreas morphology in patients with AIDS. However, additional studies were required to clarify subcellular changes. Aim: To ultrastructurally analyze pancreas changes in AIDS patients through transmission electron microscopy. Methodology and Results: Pancreas specimens for necropsy were obtained from nine consecutive AIDS patients and four normal controls. A semiquantitative histologic and ultrastructural analysis of exocrine pancreas was carried out with the following findings: preserved pancreas structure with little autolysis, marked decrease in zymogen granules (100%), increased lipofuscin pigment (80%), augmented and dilated rough endoplasmic reticulum (100%), and increased number and size of mitochondria. The Golgi complex could be identified only in two cases. In all cases, acinar nuclei were decreased in size, with peripherally condensed chromatin and undulated membrane suggesting early apoptosis. In addition, immunohistochemical evaluation of the pancreas was carried out to detect opportunistic agents. Conclusion: Decreased zymogen granules, acinar atrophy, increased lipofuscin pigment, and rarefying Golgi complex represent the morphologic substrate of protein-energy malnutrition in AIDS patients. The combination of rough endoplasmic reticulum and mitochondria changes could be due to the need for supplying vital plasma proteins rather than exportation protein synthesis associated, or not, with the deleterious effects of inflammatory cytokines and/or therapy for disease.
引用
收藏
页码:153 / 159
页数:7
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