1,634 results match your criteria: "Cystic Hygroma Imaging"
Pericardial Effusion as a Presentation of Lymphangioleiomyomatosis.
Cureus
November 2024
Internal Medicine, Unidade Local de Saúde de Braga, Braga, PRT.
Lymphangioleiomyomatosis (LAM) is a rare, systemic neoplastic disease that primarily affects women of childbearing age. The disease can arise sporadically or in association with tuberous sclerosis. It is characterized by the proliferation of abnormal smooth muscle-like cells, leading to cystic lung destruction, accumulation of chylous fluid, and development of abdominal tumors.
View Article and Find Full Text PDFSymptomatic diffuse cystic lymphangioma of the spleen in an adult: A case report.
Int J Surg Case Rep
November 2024
Department of General Surgery, Trauma and Burns Center, Ben Arous, University of Tunis El Manar, Tunisia.
Article Synopsis
- * A case study of a 54-year-old woman with chronic left upper quadrant pain led to the discovery of a 3.9 cm non-vascular splenic mass, confirmed as cystic lymphangioma through imaging and requiring laparoscopic splenectomy for symptomatic relief.
- * Though rare in adults, splenic cystic lymphangiomas can necessitate surgery if symptomatic, with imaging being crucial for diagnosis, and laparoscopic splenectomy being the preferred treatment due to its effectiveness and safety.
[Not Available].
Pan Afr Med J
November 2024
Service de Chirurgie Générale et Oncologique, Centre Hospitalier Universitaire de Beni-Messous, Alger, Algérie.
Intraperitoneal Cystic Lymphangioma (CL) is a rare benign malformative disease of lymphatic origin, with a wide range of clinical symptoms. Diagnosis is based on imaging tests and confirmed by histology. We here report the case of a 54-year-old woman presenting with chronic abdominal pain, with no effect on general condition.
View Article and Find Full Text PDFGiant benign mesenteric cysts (mesothelioma and lymphangioma): A report of two cases.
Int J Surg Case Rep
December 2024
Department of General Surgery, General Regional Hospital No 196, Edo Mex, IMSS, Mexico.
Article Synopsis
Symptomatic presentation and imaging features of a chylous cystic lymphangioma.
BMJ Case Rep
November 2024
Department of Radiology, The Johns Hopkins University School of Medicine, Baltimore, Maryland, USA
A woman in her 60s presenting with 5 days of diffuse abdominal pain was diagnosed preoperatively with a chylolymphatic mesenteric cyst. MRI and CT imaging demonstrated a 5.8 cm unilocular cyst containing a fluid-fluid level within the mesentery.
View Article and Find Full Text PDFGenetic correlation between fetal nuchal translucency thickening and cystic hygroma and exploration of pregnancy outcome.
Sci Rep
November 2024
Center of Medical Genetics, The Affiliated Yancheng Maternity and Child Health Hospital of Yangzhou University, Yancheng, 224001, Jiangsu, China.
Article Synopsis
- * In a study involving 215 pregnant women, CMA identified chromosomal abnormalities in 13% of cases, while WES detected single-gene variants in 34.3% of fetuses that had negative karyotype and CMA results.
- * The findings showed a higher incidence of adverse pregnancy outcomes in the CH group (82.9%) compared to the NT thickening group (28.2%),
Cystic lymphangioma of the head and tail of the pancreas in a middle-aged Iranian woman: A case report.
Int J Surg Case Rep
December 2024
Student Research Committee, M.D, Shiraz University of Medical Sciences, Shiraz, Iran.
Article Synopsis
Giant cystic lymphangioma as a rare cause of acute abdomen in infancy: a case report and literature review.
Folia Med (Plovdiv)
October 2024
Hippokration General Hospital of Thessaloniki, Thessaloniki, Greece.
Lymphangioma, a benign mass of lymphatic origin, primarily affects the head, neck, and oral cavity, with the abdomen being an uncommon location. Clinical presentation is defined by site of origin and size. We present the case of a 10-month-old male infant with no previous medical history, admitted to our department with diffuse abdominal pain and distension.
View Article and Find Full Text PDFPentalogy of Cantrell Marked With Ectopia Cordis, Gastroschisis, and Cystic Hygroma in the First Trimester: A Rare Case.
Cureus
September 2024
Department of Obstetrics and Gynecology, South Central Regional Medical Center, Laurel, USA.
Article Synopsis
Mesenteric cystic lymphangiomas in an 11-year-old female: A rare case report.
SAGE Open Med Case Rep
August 2024
General Surgery Department, Hama National Hospital, Hama, Syria.
Article Synopsis
- Mesenteric cystic lymphangiomas are rare, benign growths in the lymphatic system of the abdomen, mainly affecting about 1 in 250,000 people.
- Symptoms can range from not having any symptoms to severe abdominal pain, and diagnosis often involves imaging techniques like ultrasound or CT scans.
- In a case study of an 11-year-old girl, she underwent surgery to remove a confirmed cystic lymphangioma, highlighting the need to consider this condition in younger patients with abdominal masses.
Prenatal Diagnosis of Fetuses with 4q35 Deletion: Case Series and Review of the Literature.
Cytogenet Genome Res
October 2024
Genetic Metabolism Medical Center, Dalian Women and Children's Medical Center (Group), Dalian, China.
Article Synopsis
- 4q35 deletion is a rare chromosomal syndrome that presents a variety of fetal phenotypes and can be hard to detect via prenatal ultrasound.
- A study followed four fetuses with this deletion, observing conditions like fetal growth restriction, cystic hygroma, and others, noting one termination and three live births showing no major issues at one year.
- The findings suggest that while the phenotypes are diverse, fetal growth restriction is a potentially significant characteristic of 4q35 deletion cases.
NT >99th centile and cystic hygroma: Which diagnosis, which management and outcome.
J Clin Ultrasound
October 2024
Maternal Fetal Medicine Unit, University Department of Obstetrics and Gynecology "Policlinico Riuniti Foggia", Foggia, Italy.
Objectives: To evaluate the prevalence of chromosomal anomalies in fetuses affected by increased nuchal translucency(iNT >99Th centile), cystic hygroma (CH) and cases progressing to fetal hydrops (NIHF) in order to correlate this result to prognosis and perinatal fetal outcomes, improving patient's counseling.
Methods: From January 2020 to December 2023, first trimester screening according to FMF criteria were performed in "Maternal fetal medicine Unit" of Foggia's hospital. We studied and collected clinical data of fetuses affected by nuchal translucency >99th centile (iNT), CH and cases progressing to Fetal Hydrops (non-immune fetal hydrop, NIFH).
Cystic Lymphangioma of the Mesentery in an Adult: A Case Report and Literature Review.
Cureus
June 2024
Department of Surgical Oncology, Mohammed VI University Hospital, Regional Oncology Center, Faculty of Medicine and Pharmacy of Oujda, Oujda, MAR.
Article Synopsis
- Lymphangiomas are rare benign tumors that are primarily treated through surgical excision for complete removal, with diagnosis confirmed by imaging and histology.
- A case study involved a 25-year-old man who experienced abdominal pain and was found to have a large cystic mass in the mesentery, which required a surgical procedure that sacrificed part of the intestine.
- Following surgery, the patient recovered well and had no recurrence of the tumor during a three-year follow-up, highlighting the importance of complete removal to prevent complications.
[Cystic lymphangioma of the ileum].
Orv Hetil
July 2024
1 Szegedi Tudományegyetem, Szent-Györgyi Albert Orvostudományi Kar, Pathologiai Intézet Szeged, Állomás u. 1., 6725 Magyarország.
Achondrogenesis type 1B: The need for clinical vigilance in the first trimester fetus with cystic hygroma and micromelic limbs.
Taiwan J Obstet Gynecol
July 2024
Prenatal Diagnostic Center, Guangzhou Women and Children's Medical Center, Guangzhou Medical University, Guangzhou, Guangdong, China. Electronic address:
Article Synopsis
- Lymphangiomas are non-cancerous tumors from lymphatic tissue, mostly seen in kids under 2 years old, while adult cases are rare.
- A 64-year-old woman was found to have a cyst in her abdomen during a check-up, and tests revealed it was a type of lymphangioma.
- These tumors can invade other tissues, but most don’t cause symptoms, and the best way to treat them is by surgically removing them completely.
Isolated unilateral ovarian cystic lymphangioma: A case report.
Radiol Case Rep
September 2024
Department of Radio-Diagnosis, Apollo Hospitals, Jubilee Hills, Hyderabad, Telangana, 500033, India.
Article Synopsis
Cervical cystic hygroma in adults: a case report.
J Med Case Rep
July 2024
Student Research Committee, School of Medicine, Ahvaz Jundishapur University of Medical Sciences, Ahvaz, Islamic Republic of Iran.
Backgrounds: Manifestation of cystic hygroma in adulthood is very rare. The rarity of cystic hygroma in adults has caused problems in its diagnosis and management and few studies have reported cystic hygroma in adults.
Case Presentation: In this study, we reported a rare case with cervical cystic hygroma in adults.
Characteristics of adult retroperitoneal lymphangioma: a single center Chinese cohort study of 15 cases.
Discov Oncol
July 2024
Division of Hepatobiliary and Pancreatic Surgery, Department of General Surgery, The First Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, 310003, Zhejiang, China.
Article Synopsis
[Analysis of Prenatal Ultrasound Manifestations in 15 Cases of Cantrell Syndrome].
Sichuan Da Xue Xue Bao Yi Xue Ban
May 2024
（ 610045） Department of Ultrasound, Sichuan Provincial Maternity and Child Health Care Hospital, Chengdu 610045, China.
Article Synopsis
- Cantrell syndrome is a rare congenital disorder with defects in the midline abdominal wall, lower sternum, diaphragm, and an associated intracardiac defect.
- This study analyzed 15 cases of fetuses diagnosed with Cantrell syndrome using prenatal ultrasound between March 2018 and July 2023, focusing on ultrasound findings and postnatal outcomes.
- The research highlights the importance of thorough prenatal imaging for early detection and monitoring of Cantrell syndrome, which has been underrepresented in comprehensive studies.
Retroperitoneal lymphangioma in a pregnant patient: A case report and literature review.
Case Rep Womens Health
June 2024
Obstetrician and gynecologist physician, maternal fetal medicine, Obstetrics and Gynecology Department, Hospital Universitario De La Samaritana, Bogotá, Colombia.
Article Synopsis
Isolated splenic lymphangioma in adulthood.
J Surg Case Rep
June 2024
Department of General Surgery, Hera General Hospital, Al Madinah Al Munawarah Rd, Makkah 24227, Saudi Arabia.
Article Synopsis
Unusual acute right abdominal pain. Distal ileum mesenteric cystic lymphangioma in adult, a rare case and literature review.
J Surg Case Rep
May 2024
Baxshin Research Center, Baxshin Hospital, Sulaymaniyah, Kurdistan Region 46001, Iraq.
Article Synopsis
Expansion of the prenatal phenotype of Baraitser-Winter syndrome: Presentation of two cases of multiple congenital anomaly syndrome.
Am J Med Genet A
October 2024
Children's Hospital of Philadelphia, Richard D. Wood Jr. Center for Fetal Diagnosis and Treatment, Philadelphia, Pennsylvania, USA.