scholarly journals Long-term follow-up and clinical course of a rare case of von Hippel-Lindau disease: A case report and review of the literature

2016 ◽  
Vol 11 (5) ◽  
pp. 3273-3278 ◽  
Author(s):  
YU ZOU ◽  
JINGJING XU ◽  
MINMING ZHANG
Keyword(s):  
Case Report ◽  
Rare Case ◽  
Clinical Course ◽  
Review Of The Literature ◽  
Von Hippel Lindau ◽  
Long Term Follow Up ◽  
Von Hippel Lindau Disease

scholarly journals Blue Rubber Bleb Nevus Syndrome with Long-Term Follow-Up: A Case Report and Review of the Literature

2018 ◽  
Vol 2018 ◽  
pp. 1-7
Author(s):  
Hideaki Nakajima ◽  
Hiroshi Nouso ◽  
Naoto Urushihara ◽  
Koji Fukumoto ◽  
Masaya Yamoto ◽  
...  
Keyword(s):  
Clinical Course ◽  
Case Reports ◽  
Complete Resection ◽  
Review Of The Literature ◽  
Gi Tract ◽  
Short Term ◽  
Long Term Follow Up ◽  
Body Organ

Blue rubber bleb nevus syndrome (BRBNS) is a rare disease in which venous malformations (VMs) involve any body organ, most commonly the skin and the gastrointestinal (GI) tract. Treatment of BRBNS aims at preserving the GI tract as much as possible. Although there are several dozen case reports about BRBNS that describe short-term clinical courses, a few provide an account of long-term clinical course. Here, we report a case of BRBNS in a girl that required multiple abdominal surgeries due to the GI VMs and a recurrence at an interval of 14 years. The preferred approach for gastrointestinal VMs involves the complete resection of all lesions without residual VMs. It is important to bear in mind the possibility of delayed recurrence of GI VMs after surgical or endoscopic treatment.

scholarly journals Thoracoscopic and laparoscopic resection of a huge oesophageal liposarcoma: a case report

2021 ◽  
Vol 49 (9) ◽  
pp. 030006052110412
Author(s):  
Rui Li ◽  
Chen Lin ◽  
Yuxun Huang ◽  
Liang Cao ◽  
Rui Hu ◽  
...  
Keyword(s):  
Case Report ◽  
Minimally Invasive ◽  
Rare Case ◽  
Laparoscopic Resection ◽  
Polypoid Mass ◽  
Current Case ◽  
Long Term Follow Up ◽  
History Of

Oesophageal liposarcomas are particularly rare, accounting for 1.2–1.5% of all gastrointestinal liposarcomas. Surgical resection is the usual treatment. Endoscopic resection is minimally invasive but still controversial. This current case report describes a rare case of a large oesophageal liposarcoma in a 52-year-old male that presented with 10-year history of dysphagia for dry and solid food that was exacerbated by a recent common cold. Thoracoscopic and laparoscopic oesophagectomy was performed. He did not have any dysphagia or dyspnoea 1 week postoperatively. The excised specimen consisted of a polypoid mass measuring 21.0 cm × 5.1 cm. Histological examination confirmed that it was an oesophageal liposarcoma. At 1-year postoperatively, there was no sign of recurrence. Thoracoscopy and laparoscopy can be used to treat large oesophageal masses. Long-term follow-up is required as oesophageal liposarcomas tend to recur.

A “Congenitally Adapted” TFCC Tear in Radial Longitudinal Deficiency: Case Report and Review of Literature

2021 ◽  
Author(s):  
Kerstin Oestreich ◽  
T.R. Lindau
Keyword(s):  
Case Report ◽  
Wrist Arthroscopy ◽  
Review Of Literature ◽  
Review Of The Literature ◽  
Carpal Collapse ◽  
Long Term Follow Up ◽  
Radial Longitudinal Deficiency ◽  
Chronic Wrist Pain

AbstractWe present a case of chronic wrist pain in a 14-year-old child with mild radial longitudinal deficiency and radiographic carpal collapse due to the absence of the scaphoid. Wrist arthroscopy demonstrated synovitis and a tear to the TFCC, which would be called “degenerative,” according to the Palmer classification. This was debrided, and the patient is still asymptomatic at long-term follow-up. Review of the literature found one paper with a similar observation in a 17-year-old adolescent. We propose that paediatric “degenerative” tears ought to be called “congenitally adapted” tears.

Mesenteric Artery Stenosis Presenting as Severe Erosive Gastroduodenitis: A Rare Case Report With Long Term Follow-Up

2015 ◽  
Vol 6 (4) ◽  
pp. 194-196
Author(s):  
Ramesh Dwarakaprasad ◽  
Huliyurdurga Srinivasa Setty Natraj Setty ◽  
Kumarswamy X ◽  
Sunil Kumar ◽  
Guruprasad X ◽  
...  
Keyword(s):  
Case Report ◽  
Mesenteric Artery ◽  
Rare Case ◽  
Artery Stenosis ◽  
Rare Case Report ◽  
Long Term Follow Up ◽  
Mesenteric Artery Stenosis

scholarly journals Intraosseous Schwannoma (Neurilemmoma) of the Cervical Spine

Sarcoma ◽  
2001 ◽  
Vol 5 (2) ◽  
pp. 101-103 ◽  
Author(s):  
H. W. Bart Schreuder ◽  
René P. H. Veth ◽  
Maciej Pruszczynski ◽  
J. Albert M. Lemmens ◽  
Erik W. van Laarhoven
Keyword(s):  
Case Report ◽  
Cervical Spine ◽  
Local Recurrence ◽  
Review Of The Literature ◽  
Rare Tumour ◽  
Intraosseous Schwannoma ◽  
Long Term Follow Up

Purpose:To report on an extremely rare tumour located in the cervical spine, its treatment and result. Review of the literature.Patient:Case report of a 38-year-old woman with an intraosseous schwannoma of the cervical spine.Results:After local curettage no evidence for local recurrence at long-term follow-up.

Congenital Lateral Palatal Synechia Associated With Cleft Palate: A Case Report With Long-Term Follow-Up and Review of the Literature

2019 ◽  
Vol 57 (6) ◽  
pp. 778-781
Author(s):  
Yoshimichi Imai ◽  
Masahiro Tachi
Keyword(s):  
Case Report ◽  
Literature Review ◽  
Oral Cavity ◽  
Cleft Palate ◽  
Review Of The Literature ◽  
Long Term Follow Up ◽  
Long Term Prognosis ◽  
Cavity Floor

Lateral palatal synechiae are rare congenital adhesions running from the free borders of the cleft palate to the lateral parts of the tongue or the oral cavity floor, typically found in cleft palate lateral synechiae syndrome. We present a case of congenital lateral palatal synechia associated with a cleft palate that we treated and followed up for 10 years. We present the long-term prognosis. We also discuss variations in intraoral synechiae associated with cleft palate and the etiology of lateral palatal synechiae through a literature review.

Sign in / Sign up

Export Citation Format

Share Document