Results 201 to 210 of about 18,426,765 (306)

Gastric Metastasis of Uterine Leiomyosarcoma Detected During Surveillance Endoscopy and Resected by Endoscopic Submucosal Dissection After Multiple Metachronous Metastases: A Case Report

DEN Open, Volume 7, Issue 1, April 2027.
ABSTRACT Uterine leiomyosarcoma (uLMS) is a rare, aggressive uterine malignancy that usually metastasizes hematogenously, whereas gastrointestinal involvement is uncommon. A 69‐year‐old woman with uLMS treated by hysterectomy and adjuvant chemotherapy developed metachronous lung, sigmoid colon, gallbladder, and abdominal wall metastases.
Yuiko Nagasawa, Takahiro Hiratsuka, Daisuke Minezaki, Wataru Miyoshino, Ryo Ogawa, Tomonori Akagi, Hidefumi Shiroshita, Yoshitake Ueda, Kazuhiro Mizukami, Masafumi Inomata   +9 more
wiley   +1 more source

Type B aortic dissection.

Annals of cardiothoracic surgery, 2014
Christopher G, Harris, Beth, Croce, David H, Tian   +2 more
openaire   +1 more source

A Case of High-Risk Acute Stanford Type B Aortic Dissection in a Right-Sided Aortic Arch Presenting With Transient Hemiparesis. [PDF]

Cureus
Chamma AG, Saliba W, Chamma L.
europepmc   +1 more source

Computed tomographic characterisation and surgical management of a caudal mediastinal paraoesophageal abscess with associated pneumonia in a dog

Veterinary Record Case Reports, Volume 14, Issue 4, November 2026.
Abstract An 8‐year‐old, entire, male German shorthaired pointer presented with acute respiratory distress, pyrexia and coughing following a period of boarding. Thoracic radiographs identified a caudal mediastinal mass effect with severe multilobar bronchopneumonia.
Yi Gu, Kyle L. Granger Jr., Alyson Frederick, Laura Roy‐Eitner, Stephanie Kline   +4 more
wiley   +1 more source

Acute Respiratory Distress Syndrome as a Rare but Potentially Fatal Complication of Acute Type B Aortic Dissection: A Case Report. [PDF]

Cureus
Erregui H, Moujahid M, Madouim H, Houba A, Doghmi N.   +4 more
europepmc   +1 more source

Clinical Outcomes and Patient Experiences With Celiprolol Therapy in Vascular Ehlers–Danlos Syndrome: The First Non‐European Cohort

American Journal of Medical Genetics Part A, Volume 200, Issue 10, Page 2241-2249, October 2026.
ABSTRACT Vascular Ehlers–Danlos syndrome (vEDS) is a hereditary connective tissue disorder caused by heterozygous pathogenic variants in COL3A1. European studies have shown that celiprolol may reduce the risk of life‐threatening vascular events, but outcomes in non‐European populations and the therapy's psychological impact remain unclear. We conducted
Megumi Furuhata‐Yoshimura, Tomomi Yamaguchi, Tomoki Kosho   +2 more
wiley   +1 more source

Psychological experiences of patients with Stanford type B aortic dissection during the preoperative waiting period: a qualitative study. [PDF]

BMC Cardiovasc Disord
Liu C, Xie X, Hu A, Qi W, Su Y, Zhang P.
europepmc   +1 more source

Does salinity make a difference—Kidney anatomy of Saimaa (Pusa saimensis) and Baltic ringed seals (Pusa hispida botnica)

The Anatomical Record, Volume 309, Issue 10, Page 2948-2961, October 2026.
Abstract As habitat salinity markedly differs between the endangered, freshwater‐dwelling Saimaa ringed seal (Pusa saimensis Nordquist, 1899) and the brackish water‐inhabiting Baltic ringed seal (Pusa hispida botnica Gmelin, 1788), we investigated whether this difference has resulted in morphological changes to their kidneys.
Heini Nihtilä, Juha Laakkonen
wiley   +1 more source

Catheter-Based Renal Denervation in Acute Type B Aortic Dissection to Optimize Long-Term Pressure Control. [PDF]

JACC Case Rep
Baresi GF, Melloni A, Bonardelli S, Bertoglio L.   +3 more
europepmc   +1 more source

Cancer Risk in Marfan Syndrome: A Swedish Population‐Based Cohort Study

International Journal of Cancer, Volume 159, Issue 7, Page 1707-1714, 1 October 2026.
The cancer risk in Marfan syndrome, an autosomal dominant connective tissue disorder, largely remains to be explored. In this population‐based matched cohort study of 1544 Swedish patients, the overall cancer risk in adults with Marfan syndrome showed no significant increase, except for the risk of endocrine tumours with a nearly threefold increase ...
Ida Nordgren, Anna Skarin Nordenvall, Alexandra Wachtmeister, Fulya Taylan, Yunxia Lu, Christina Norrby, Anna Lindstrand, Giedre Grigelioniene, Giorgio Tettamanti   +8 more
wiley   +1 more source