Advances in the Diagnosis and Treatment of Hepatogastroenterology

A special issue of Diagnostics (ISSN 2075-4418). This special issue belongs to the section "Pathology and Molecular Diagnostics".

Deadline for manuscript submissions: closed (31 July 2023) | Viewed by 4614

Special Issue Editor


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Guest Editor
Department of Gastroenterology, Changhua Christian Hospital and Yuan-Lin branch Department of Hospitality Management, MingDao University, Changhua, Taiwan
Interests: primary hepatic angiosarcoma; deep enteroscopy; pneumatosis intestinalis and portal vein air; acute abdomen; refractory gastrointestinal bleeding

Special Issue Information

Dear Colleagues,

Advances in the diagnosis and treatment of hepatogastrointestinal diseases have been remarkable in the recent years. Imaging in the diagnosis of gastrointestinal diseases, for example, has seen advances such as chromoendoscopy, upper and lower gastrointestinal endoscopy with artificial intelligence (AI) apply, capsule endoscopy, deep enteroscopy, and endoscopic ultrasound. Imaging in the diagnosis of hepatology has also seen significant advances, including color ultrasound with contrast, abdominal multidetector computed tomography, and advanced magnetic resonance imaging.

Surgery continues to play a major role in the treatment of hepatogastrointestinal disease, especially in cases of advanced malignancy. The introduction of multimodal therapy, including target therapy and immuno-oncology (I-O) therapy, has dramatically improved the chance of survival of advanced malignancy.

It is my pleasure to invite authors to submit your contributions to this Special Issue. This Special Issue will focus on the diagnosis and treatment of hepatogastrointestinal diseases.

Invited topics may include:

  • New diagnostic imaging and therapeutic capabilities in hepatic diseases;
  • New diagnostic imaging and therapeutic capabilities in gastroenterology diseases.

Prof. Dr. Yangyuan Chen
Guest Editor

Manuscript Submission Information

Manuscripts should be submitted online at www.mdpi.com by registering and logging in to this website. Once you are registered, click here to go to the submission form. Manuscripts can be submitted until the deadline. All submissions that pass pre-check are peer-reviewed. Accepted papers will be published continuously in the journal (as soon as accepted) and will be listed together on the special issue website. Research articles, review articles as well as short communications are invited. For planned papers, a title and short abstract (about 100 words) can be sent to the Editorial Office for announcement on this website.

Submitted manuscripts should not have been published previously, nor be under consideration for publication elsewhere (except conference proceedings papers). All manuscripts are thoroughly refereed through a single-blind peer-review process. A guide for authors and other relevant information for submission of manuscripts is available on the Instructions for Authors page. Diagnostics is an international peer-reviewed open access semimonthly journal published by MDPI.

Please visit the Instructions for Authors page before submitting a manuscript. The Article Processing Charge (APC) for publication in this open access journal is 2600 CHF (Swiss Francs). Submitted papers should be well formatted and use good English. Authors may use MDPI's English editing service prior to publication or during author revisions.

Keywords

  • primary hepatic angiosarcoma 
  • deep enteroscopy 
  • pneumatosis intestinalis and portal vein air 
  • acute abdomen 
  • refractory gastrointestinal bleeding

Published Papers (3 papers)

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6 pages, 11222 KiB  
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Unusual Rapid Growth of Primary Splenic Diffuse Large B-Cell Lymphoma with Extensive Necrosis
by Yue-Ren Chen, Hwa-Koon Wu and Yang-Yuan Chen
Diagnostics 2023, 13(1), 35; https://doi.org/10.3390/diagnostics13010035 - 22 Dec 2022
Viewed by 1323
Abstract
The primary splenic lymphoma is extremely uncommon with an incidence rate of <1% of all the lymphomas under the strict criteria for diagnosis expounded by Das Gupta et al. Clinical presentations of nonspecific symptoms are weight loss, weakness, fever, and left upper quadrant [...] Read more.
The primary splenic lymphoma is extremely uncommon with an incidence rate of <1% of all the lymphomas under the strict criteria for diagnosis expounded by Das Gupta et al. Clinical presentations of nonspecific symptoms are weight loss, weakness, fever, and left upper quadrant pain or discomfort due to enlarged spleen. Abdominal ultrasound and CT are the most widely used imaging modality for the assessment of lymphoma. The imaged features of splenic lymphoma are nonspecific; typical lymphoma presents as a diffusely enlarged spleen. The abdominal CT scan in our case showed a large cystic splenic mass measuring 14 cm without enhancement after contrast medium. Lymphoma is often described as an aggressive tumor because its rapid doubling time can quickly increase the size of a tumor. In our case, the tumor grew to more than 100 times its original size in 4 months. So, we present this unusual rapid growth of primary splenic lymphoma. Full article
(This article belongs to the Special Issue Advances in the Diagnosis and Treatment of Hepatogastroenterology)
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4 pages, 5414 KiB  
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Multiple Synchronous Mucosa-Associated Lymphoid Lymphomas Involving in the Stomach, Duodenum, Ileum, and Sigmoid
by Chun-Wei Chen, Yang-Yuan Chen and Yung-Fang Chen
Diagnostics 2022, 12(12), 3150; https://doi.org/10.3390/diagnostics12123150 - 13 Dec 2022
Viewed by 1111
Abstract
Gastric MALToma is an extra-nodal marginal-type B-cell lymphoma. MALToma may occur secondary to chronic inflammation and autoimmunity. The most common gastrointestinal (GI) site of MALToma is the stomach, with approximately 50% of lesions occurring there. Synchronous upper and lower GI MALTomas rarely occur, [...] Read more.
Gastric MALToma is an extra-nodal marginal-type B-cell lymphoma. MALToma may occur secondary to chronic inflammation and autoimmunity. The most common gastrointestinal (GI) site of MALToma is the stomach, with approximately 50% of lesions occurring there. Synchronous upper and lower GI MALTomas rarely occur, with few cases reported. We present the case of a 67-year-old patient who presented asymptomatic and was found to have synchronous multifocal upper and lower GI MALTomas in the stomach, duodenum, terminal ileum, and sigmoid, which did not respond to H. Pylori eradication therapy. Full article
(This article belongs to the Special Issue Advances in the Diagnosis and Treatment of Hepatogastroenterology)
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4 pages, 8944 KiB  
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Migration of a Retained Surgical Suture Needle in the Common Bile Duct
by Tzu-Cheng Wen, Kuo-Hua Lin and Yang-Yuan Chen
Diagnostics 2022, 12(10), 2276; https://doi.org/10.3390/diagnostics12102276 - 21 Sep 2022
Cited by 1 | Viewed by 1581
Abstract
Retained surgical foreign bodies have been a cause of concern since physicians began operating on patients. Retained surgical foreign bodies in the common bile duct (CBD) are rare and may cause cholangitis and jaundice. We report the case of a patient who initially [...] Read more.
Retained surgical foreign bodies have been a cause of concern since physicians began operating on patients. Retained surgical foreign bodies in the common bile duct (CBD) are rare and may cause cholangitis and jaundice. We report the case of a patient who initially presented with fever and right upper-quadrant abdominal pain. He had received cholecystectomy and choledochojejunostomy 28 years ago and had been well since then. Abdominal computed tomography (CT) revealed left-lobe liver abscess and a linear curve of high-density material. Endoscopic retrograde cholangiopancreatography (ERCP) displayed mild dilatation of the common bile duct (CBD) and choledojejunostomic fistula of the middle CBD. A curved, linear, rusty, metallic surgical suture needle was detected and successfully removed under ERCP. Full article
(This article belongs to the Special Issue Advances in the Diagnosis and Treatment of Hepatogastroenterology)
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