HIV disease and the gastrointestinal tract

Author(s):  
Daniel Marks ◽  
Marcus Harbord

General principles Luminal disease Pancreatitis Hepatobiliary disease HIV-infected patients with low CD4 counts frequently develop acute GI and hepatobiliary disease. Whilst susceptible to the same disorders as immunocompetent patients, the differential diagnosis is broader. The aim is to identify treatable disorders. Clinical presentations are rarely specific, and patients usually require investigation rather than empiric treatment....

1994 ◽  
Vol 5 (suppl e) ◽  
pp. 34E-39E ◽  
Author(s):  
Julio Sg Montaner ◽  
Leila Spour ◽  
Carlos Zala

Pneumocystis carinii pneumonia (PCP) and Kaposi’s sarcoma were the harbingers of the HIV epidemic more than 10 years ago. Since then. the spectrum of pulmonary disease associated with HIV infection has become better understood. Although most of these conditions are infectious in nature. neoplastic and inflammatory processes also occur with increased frequency. The most common infectious pulmonary diseases include PCP. Mycobacterium tuberculosis infection and pyogenic bacterial pneumonia secondary to Streptococcus pneumoniae. Haemophilus influenzae or Staphylococcus aureus. Among the noninfectious causes of pulmonary disease. the most common are Kaposi's sarcoma. airways hyper-reactive disease (asthma) and emphysema. Respiratory involvement in HIV-infected individuals is not always related to the HIV infection. These patients often present with pulmonary disorders that are common in the genernal population. Differential diagnosis of respiratory conditions is significantly facilitated by the prior knowledge of the degree of immunodeficiency present as measured by the CD4 count. In particular, most episodes of PCP occur in patients with absolute CD4 counts below 200 cells/mm3. On the other hand. bacterial pneumonias and tuberculosis tend to occur at any time during the natural history of HIV disease. History and physical examination can help in the differential diagnosis; however. they are rclatively nonspecific in this setting. The same can be said of radiographic findings as well as laboratory and physiological abnormalities. Of note, the lactate dehydrogenase (LDH) serum level has proved to be extremely useful in ruling out PCP. Even mild PCP is usually accompanied by a significant elevation of LDH. Furthermore, the degree of LDH elevalion generally correlates wilh the severity of the PCP episode. Also, changes in LDH parallel the clinical course of the underlying PCP. Often LDH level has been useful in discriminating worsening PCP following the initiation of therapy from worsening respiratory symptoms due to superimposed disease. It must be emphasized, however. thal LDH level. although a very sensitive marker for PCP. is also nonspecific. Of note, hemolysis, lymphomas, pulmonary embolism, liver disease and dapsone therapy can be associated with elevated LDH in the context of HIV disease. Given the high frequency of respiratory involvement in this patient populalion. it is generally recommended thal preventive therapies be used whenever possible. Current recommendations stress the need for pneumococcal vaccine, yearly flu vaccination and routine screening with tuberculin skin test (PPD). HIV-infected individuals with a PPD skin test reaction of 5 mm of induration or greater using 5 tuberculin units will be considered candidates for one year of isoniazid prophylaxis. PCP prophylaxis has been shown to be extremely useful in this selling either as primary or secondary prophylaxis. Recently. rifabutin at doses of 300 mg daily has been shown to decrease significantly the frequency of Mycobacterium avium complex infection in patients with CD4 counts below 100/mm3. (Pour résumé. voir page 35E)


2013 ◽  
Vol 2013 ◽  
pp. 1-3 ◽  
Author(s):  
Sarah Alghamdi ◽  
Yumna Omarzai

Malignant melanoma of the gastrointestinal tract is an uncommon neoplasm that could be primary or metastatic. Small intestine represents the most common site for the metastatic melanoma; however, it could be found anywhere in the gastrointestinal tract. Intussusception is a rare cause of intestinal obstruction in adults compared to children. In 90% of the cases, the underlying cause can be found, and in 65% of the cases, intussusception is caused by the neoplastic process. The majority of the neoplasms are benign, and about 15% are malignant. Metastatic melanoma is one of the most common metastatic malignancies to the gastrointestinal tract; however, the premortem diagnosis is rarely made. Here, we report an uncommon clinical presentation of metastatic melanoma causing intussusception in an 80-year-old man. This diagnosis should be considered in a differential diagnosis in any patient who presents with gastrointestinal symptoms and a history of melanoma.


2015 ◽  
Vol 139 (1) ◽  
pp. 133-139 ◽  
Author(s):  
Jaclyn F. Hechtman ◽  
Noam Harpaz

Primary neurogenic gastrointestinal polyps are encountered relatively frequently in routine pathology practice. They encompass a variety of neoplastic entities with clinical, morphologic, and molecular features that reflect the diversity of neural elements within the gastrointestinal system. Although most are benign and encountered incidentally, accurate diagnosis may have important clinical implications because of the associations of certain neurogenic polyps with familial syndromes or other conditions. We review the pathology of these polyps with an emphasis on the diagnostic challenges that they pose and on newly described subtypes.


2021 ◽  
Vol 2021 ◽  
pp. 1-20
Author(s):  
Shivantha Amarnath ◽  
Liliane Deeb ◽  
Jobin Philipose ◽  
Xiaomin Zheng ◽  
Vivek Gumaste

A granuloma is defined as a localized inflammatory reaction or a hypersensitive response to a nondegradable product leading to an organized collection of epithelioid histiocytes. Etiologies of granulomatous disorders can be divided into two broad categories: infectious and noninfectious (autoimmune conditions, toxins, etc.) causes. The endless list of causalities may prove challenging for gastroenterologists and pathologists to formulate a list of clearly defined differentials. This is true when distinguishing these etiologies based on various clinical presentations and endoscopic and histological findings. We aim to provide a comprehensive review of some of the frequent and rare infectious granulomatous diseases of the gastrointestinal tract documented in the literature to date. We provide an overview of each infectious pathology with an emphasis on epidemiology, clinical presentation, and endoscopic and histologic findings, in addition to treatment.


2021 ◽  
Vol 2021 (2) ◽  
pp. 68-71
Author(s):  
R.I. Khalafova ◽  

To study the frequency of detection of combinations of the main syndromes of the gastrointestinal tract (GIT) and their differential diagnosis, consisting of irritable bowel syndrome (IBS), syndrome of functional dyspepsia (SFD), chronic idiopathic dyspepsia (CIT) and gastroesophageal reflux disease (GERD). The main gastrointestinal syndromes are quite often detected among different groups of military personnel and members of their families. ES plays an important role in their formation. International recommendations allow anamnestic diagnosis of each of the syndromes in separately and in combination with each other. The medical appealability of patients depends on the severity of the symptoms of the syndromes, it is most pronounced when they are combined.


1986 ◽  
Vol 67 (6) ◽  
pp. 441-444
Author(s):  
R. F. Akberov

Functional disorders of the gastrointestinal tract in young children are the most difficult and insufficiently studied issues of clinical medicine. So far, such relevant issues as the mechanism of regurgitation and vomiting, the origin of pylorostenosis and dyskinetic disorders of the small intestine have not been elucidated. Unified methods of diagnosis and differential diagnosis of both functional and organic changes of the gastrointestinal tract, especially in children in the first days of life, have not been developed.


Author(s):  
James Wood

The reaction of most students to questions about hepatobiliary dis­ease is a sinking feeling of despair! ‘Lots of biochemistry and anatomy together with a bunch of funny eponymous syndromes to remember!’ Well, hepatobiliary disease is remarkably logical; knowledge of the basic principles of biliary metabolism and the key anatomical facts is usually more than enough if it is coupled with a sound appreciation of the com­mon clinical presentations. These presentations are extremely common; most days on call will see the surgical team looking after at least one patient with one of the range of hepatopancreaticobiliary problems that can present as an emergency. This chapter will review the basic principles of liver and pancreatic disease and the anatomy that goes with it. Both elective and emergency surgical presentations will also be covered, allowing you to revise knowl­edge of key clinical presentations in practice.


2019 ◽  
Vol 1 (3) ◽  
Author(s):  
Jonah N Rubin ◽  
Lauren A George ◽  
Raymond K Cross ◽  
Uni Wong

Abstract Intestinal sarcoidosis can mimic Crohn disease (CD), and it is important to evaluate for alternative diagnoses in patients who present with atypical symptoms or do not respond to conventional therapy. Furthermore, CD, with or without biologic therapy, has been associated with neurological symptoms including neuropathies, myelopathies, thromboembolic, and demyelinating diseases leading to diagnostic uncertainty. We present a case of sarcoidosis of the luminal gastrointestinal tract and central nervous system, which mimicked the presentation of CD. This case highlights the need to expand the differential diagnosis in patients who present with atypical symptoms and do not respond to biologic therapy.


2019 ◽  
Vol 34 (11) ◽  
pp. 1989-1993
Author(s):  
Yanhua Zhou ◽  
Yanlin Zhang ◽  
Haiying Zhao ◽  
Xuan Cui ◽  
Yongqiu Wei ◽  
...  

Abstract Introduction Epstein-Barr virus (EBV)–associated lymphoproliferative diseases (LPD) with digestive tract involvement in immunocompetent patients is rather rare. Since the symptoms of EBV-associated LPD involving the gastrointestinal tract in immunocompetent patients are similar to those of inflammatory bowel disease (IBD), most patients are initially misdiagnosed. Case presentation In this paper, we present two cases of EBV-associated T cell LPD involving the colon in immunocompetent patients and review the relevant literature. Conclusion EBV serological testing may help in detecting this disease, and our findings suggest that histopathological evidence of EBV, such as the Epstein-Barr encoding region, is very important to establish the diagnosis.


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