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Lymphangioma

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https://www.readbyqxmd.com/read/28629796/large-omental-cystic-lymphangioma-masquerading-as-mucinous-ovarian-neoplasia-in-an-8-year-old-premenarchal-girl-the-findings-from-diagnostic-imaging-and-laparoscopic-assisted-excision
#1
Akihiro Takeda, Hiroaki Ito, Hiromi Nakamura
BACKGROUND: Omental cystic lymphangioma is an extremely rare abdominal mass caused by congenital malformation. CASE: An 8-year-old premenarchal girl reported abdominal pain. Diagnostic imaging revealed a large multicystic mass measuring 22 cm in diameter, which occupied the entire abdominal cavity with ascites. Emergency laparoscopy revealed a ruptured large cystic mass originating from the greater omentum; this was followed by successful laparoscopic-assisted excision...
June 16, 2017: Journal of Pediatric and Adolescent Gynecology
https://www.readbyqxmd.com/read/28597093/-pediatric-salivary-gland-tumors-and-tumor-like-lesions
#2
REVIEW
A Agaimy, H Iro, J Zenk
Salivary gland tumors and tumor-like lesions in the pediatric population are uncommon. They comprise a heterogeneous group of infectious/inflammatory and neoplastic conditions. Pediatric salivary neoplasms include benign tumors of mesenchymal or epithelial origin as well as malignancies of epithelial (carcinomas), mesenchymal (sarcoma) or hematolymphoid (lymphoma) derivation. Infectious/inflammatory conditions and hematolymphoid malignancies may represent either genuine parenchymal pathology or conditions involving intraglandular lymph nodes of the parotid glands (intraglandular lymphadenopathy and intraglandular nodal lymphomas)...
June 9, 2017: Der Pathologe
https://www.readbyqxmd.com/read/28595986/oral-foregut-duplication-cysts-a-rare-and-fascinating-congenital-lesion-case-report-and-review-of-the-literature
#3
Kurt J Knowles, Juraj Berkovic, Anil Gungor, Majd Al Shaarani, Valerie Lockhart, Firas Al-Delphi, Elba A Turbat-Herrera
Oral foregut duplication cysts are extremely rare lesions with approximately 57 cases reported. They are congenital cysts, located in the anterior or ventral tongue, and occur predominantly in males. They are lined by one or more types of epithelia which is limited to gastric, intestinal or respiratory epithelium. The differential diagnosis includes lymphangioma, hemangioma, ranula, epidermoid cyst, teratoma and less likely a malignant process.
November 23, 2016: American Journal of Otolaryngology
https://www.readbyqxmd.com/read/28579136/role-of-intralesional-bleomycin-in-orbital-lymphangioma-a-prospective-study
#4
Dr Nirav D Raichura, Dr Md Shahid Alam, Dr Veena Noronha, Dr Bipasha Mukherjee
AIM: To evaluate the efficacy of intralesional bleomycin injection in management of lymphangiomas of the orbit. METHODS: This prospective non-comparative interventional case study included 13 patients with orbital lymphangiomas. Reconstituted bleomycin 1 to 5 ml (0.5 IU/ kg body weight; maximum 15 IU/ml) was injected together with 2% lignocaine in the lesion as seen on imaging or under ultrasound guidance in deeper lesions. Repeat injections were given as and when required after every 4 weeks...
June 1, 2017: Journal of AAPOS: the Official Publication of the American Association for Pediatric Ophthalmology and Strabismus
https://www.readbyqxmd.com/read/28536213/non-surgical-treatment-of-a-relapsed-cystic-hygroma-in-an-adult
#5
Rafael García Carretero, Belen Rodriguez-Maya, Oscar Vazquez-Gomez
Lymphatic malformations, also known as lymphangiomas or cystic hygromas, are benign masses that typically affect newborns and infants and involve the head and neck regions. They are, however, rare in adults and even rarer in the axillary region. Although surgery is considered to be the treatment of choice, we present a rare case of a recurrent cystic hygroma 32 years after the first surgical operation. Due to the cosmetic concerns and the risks of a surgical approach, non-surgical therapy with percutaneous sclerosants was performed, with a good outcome after a 2-year follow-up period...
May 22, 2017: BMJ Case Reports
https://www.readbyqxmd.com/read/28534344/orbital-lymphangioma-characteristics-and-treatment-outcomes-of-12-cases
#6
Young Jun Woo, Chang Yeom Kim, Bradford Sgrignoli, Jin Sook Yoon
PURPOSE: To report the patient characteristics and treatment outcomes in 12 cases of orbital lymphangioma. METHODS: In this study, orbital lymphangioma was diagnosed based on clinical, radiologic (computed tomography, magnetic resonance imaging), and histologic findings when possible. Patients whose vision was not compromised by orbital lymphangioma, or that did not have increased intraocular pressure (IOP), received oral corticosteroids. Orbital lymphangioma that affected vision or increased IOP was treated by surgery, which included aspiration of blood or partial resection with or without injection of a sclerosant...
June 2017: Korean Journal of Ophthalmology: KJO
https://www.readbyqxmd.com/read/28523092/management-of-a-life-threatening-bleeding-following-extraction-of-deciduous-second-molar-related-to-a-capillary-haemangioma
#7
REVIEW
Amr Amin Ghanem, Yasser Nabil El Hadidi
Various forms of vascular lesion affect the head and neck region. The head and neck vascular lesions are classified into neoplasms and malformations. Neoplasm presents either as hemangioma or lymphangioma; neoplasm usually presents in young age compared with vascular malformation. A 9-year-old female patient presented to the outpatient clinic referred from the department of pedodontics after extraction of a right mandibular second deciduous molar. Extraction was done by dental GP in outpatient clinic. Massive bleeding followed the extraction...
June 2017: Craniomaxillofacial Trauma & Reconstruction
https://www.readbyqxmd.com/read/28520318/-image-of-the-month-a-pediatric-case-of-unilateral-proptosis-and-cystic-lymphangioma
#8
L Adouane, Ch Chantrain, M Lewin, P Philippet, M Thimmesch
No abstract text is available yet for this article.
May 2017: Revue Médicale de Liège
https://www.readbyqxmd.com/read/28515992/dermoscopy-of-cutaneous-lymphangioma-circumscriptum
#9
Abhijeet K Jha, Aimilios Lallas, Sidharth Sonthalia
Lymphangiomas are congenital lymphatic malformations. They are clinically characterized by clusters of translucent vesicles, and on dermoscopy, yellow lacunae surrounded by pale septa as well as reddish to bluish lacunae have been described. A young male presented with a seven-year history of a vesicular lesion. Dermoscopy revealed multiple white-yellowish well-circumscribed roundish areas (lacunae) surrounded by pale septa. A few lacunae contained blood, which was characteristically accumulated in the lowest part of the lacuna, resulting in an appearance similar to the so-called "hypopyon" of the eye...
April 2017: Dermatology Practical & Conceptual
https://www.readbyqxmd.com/read/28512390/cystic-lymphangioma-of-the-colon-endoscopic-removal-beyond-the-frontiers-of-size
#10
Kanthi Rekha Badipatla, Chaitanya Chandrala, Puvanalingam Ayyadurai, Madhavi Biyyam, Binita Sapkota, Masooma Niazi, Suresh Kumar Nayudu
Cystic lymphangiomas are benign colonic neoplasms arising from the submucosa. Traditionally, endoscopic resection has been described for smaller lesions, while surgery is reserved for larger symptomatic lesions. We present a case of a 69-year-old asymptomatic individual noted to have a cystic lymphangioma of the colon measuring 5 cm, which was successfully removed with endoloop endoscopic resection without any complications.
January 2017: Case Reports in Gastroenterology
https://www.readbyqxmd.com/read/28477401/management-of-a-large-cystic-lymphangioma-causing-intestinal-obstruction
#11
Michael J O'Grady, Josephine O'Grady
No abstract text is available yet for this article.
May 5, 2017: ANZ Journal of Surgery
https://www.readbyqxmd.com/read/28458827/a-mesocolonic-lymphangioma-in-an-adult-with-peritonitis-a-case-report
#12
Yuzo Hirata, Yuzo Okamoto, Hirofumi Nakayama, Eiji Ono
Cystic lymphangiomas of the mesocolon are very rare in adults. They are usually asymptomatic, but can present with an acute abdomen. We report an adult patient with cystic lymphangioma of the mesocolon that manifested with peritonitis. A 33-year-old man presented with fever and severe pain with muscle guarding in the left abdomen. Laboratory data indicated high-grade inflammation. Enhanced computed tomography (CT) showed multiple low-density masses with peripherally enhancing rims, strongly suspicious for cysts, in the left abdomen...
February 2017: Journal of Surgical Case Reports
https://www.readbyqxmd.com/read/28455093/-giant-mesocolic-cystic-lymphangioma-a-treacherous-prenatal-presentation-case-report
#13
J Chevreau, P Naepels, P Buisson, L Razafimanantsoa, J Gondry, E Haraux
Cystic lymphangiomas are usually located in the neck region. Less frequently, they can be found in the abdomen. In those cases, pre- and neonatal diagnosis is extremely difficult. We report on the case of a giant mesocolic cystic lymphangioma, diagnosed at birth, in a child who had been monitored during the prenatal period for what was believed to be a digestive dilatation. The progression was marked by excellent tolerance despite a complete lack of regression in the first 10 months of life. The authors discuss the prenatal signs that should suggest this diagnosis and an MRI, as well as management during the 1st year of life...
April 25, 2017: Archives de Pédiatrie: Organe Officiel de la Sociéte Française de Pédiatrie
https://www.readbyqxmd.com/read/28451011/cystic-lymphangioma-in-a-44-year-old-woman
#14
Moncef Sellami, Abdelmonem Ghorbel
No abstract text is available yet for this article.
2017: Pan African Medical Journal
https://www.readbyqxmd.com/read/28440897/sonographic-findings-in-two-cases-of-lymphangioma-of-the-mesocolon-in-adults
#15
Hiroko Naganuma, Hideaki Ishida, Tomoya Komatsuda, Mayu Hakamada, Toshiya Sawada, Rika Satoyoshi, Katsuhiko Enomoto, Takaharu Miyauchi
Lymphangioma of the mesocolon is very rare. We report two cases of surgically resected and histologically proven mesocolic lymphangioma in adults. In both cases, ultrasound revealed a large cystic mass with multiple thin septa in the lower abdomen. A peculiar finding was the large craniocaudal sliding movement of the mass synchronized with the patient's respiration, which was a clue to the diagnosis of mesenteric lymphangioma. © 2017 Wiley Periodicals, Inc. J Clin Ultrasound, 2017.
April 25, 2017: Journal of Clinical Ultrasound: JCU
https://www.readbyqxmd.com/read/28440240/cystic-pancreatic-lymphangioma-diagnosed-with-endoscopic-ultrasound-guided-fine-needle-aspiration
#16
Ikram Hussain, Tiing Leong Ang
Pancreatic lymphangiomas are rare, but benign neoplasms. Historically, the diagnoses in various case reports were mostly made after surgical resection. There are emerging data concerning the utility of endoscopic ultrasound-guided fine needle aspiration (EUS-FNA) to differentiate it from more sinister pancreatic cystic neoplasms. A confident preoperative diagnosis with EUS-FNA is crucial to avoid unnecessary workup or surgery, especially for small and asymptomatic lesions. Here, we present a rare case of asymptomatic pancreatic lymphangioma which was diagnosed with EUS-FNA...
March 2017: Endoscopic Ultrasound
https://www.readbyqxmd.com/read/28430735/sodium-tetradecyl-sulfate-a-review-of-clinical-uses
#17
Helena A Jenkinson, Kelly M Wilmas, Sirunya Silapunt
BACKGROUND: Sodium tetradecyl sulfate (STS) is Food and Drug Administration approved for treatment of varicose veins, but numerous other off-label applications have been reported. OBJECTIVE: To describe the clinical uses of STS, as well as efficacy and adverse effects. METHODS: Review of studies searchable on PubMed from 1938 to 2016 describing clinical uses of STS to determine efficacy and adverse effects associated with various applications...
April 19, 2017: Dermatologic Surgery: Official Publication for American Society for Dermatologic Surgery [et Al.]
https://www.readbyqxmd.com/read/28420514/detection-of-mosaic-15q11-1-q11-2-deletion-encompassing-nbeap1-and%C3%A2-poteb-in-a-fetus-with-diffuse-lymphangiomatosis
#18
Chih-Ping Chen, Kuo-Gon Wang, Hsu-Kuang Huang, Cheng-Ran Peng, Schu-Rern Chern, Peih-Shan Wu, Yen-Ni Chen, Shin-Wen Chen, Chen-Chi Lee, Wayseen Wang
OBJECTIVE: We present cytogenetic and molecular cytogenetic diagnoses of mosaic deletion of chromosome 15q11.1-q11.2 in a fetus with diffuse lymphangiomatosis. CASE REPORT: A 33-year-old woman underwent amniocentesis at 22 weeks of gestation because of fetal diffuse lymphangiomatosis involving left-side chest, abdominal cavity, thigh and vulva, and intrauterine growth restriction. Amniocentesis revealed a karyotype of 46,XX,del(15) (q11.1q11.2)[9]/46,XX[26]. The mother had a karyotype of 46,XX...
April 2017: Taiwanese Journal of Obstetrics & Gynecology
https://www.readbyqxmd.com/read/28419699/cystic-mesenteric-lymphangioma-a-case-report
#19
Pramod Durgakeri, Beth Penington
No abstract text is available yet for this article.
April 16, 2017: ANZ Journal of Surgery
https://www.readbyqxmd.com/read/28408932/huge-lymphangioma-of-the-esophagus-resected-by-endoscopic-piecemeal-mucosal-resection
#20
Dinghai Luo, Liping Ye, Weidan Wu, Haihong Zheng, Xinli Mao
We present an unusual case of a 41-year-old male patient with a large lymphangioma of the esophagus. Endoscopy revealed that the structure measured 60 × 10 mm in the mucosa and the submucosa and had a heterogenous echo pattern. The esophageal mass was successfully resected by endoscopic piecemeal mucosal resection. However, most esophageal lymphangiomas that are larger than 2 cm in diameter reported in the literature can be removed only through open surgery. Thus far, we know of no reported cases of endoscopic resection as a treatment for this case...
2017: Case Reports in Medicine
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