2.Primary Idiopathic Chylopericardium Associated with Cervicomediastinal Cystic Hygroma.
Byoung Chul CHO ; Seok Min KANG ; Seung Chul LEE ; Jeong Geun MOON ; Dong Hyung LEE ; Sang Hyun LIM
Yonsei Medical Journal 2005;46(3):439-444
Chylopericardium is a rare clinical entity in which chylous fluid accumulates in the pericardial cavity. We report a case of primary idiopathic chylopericardium associated with multiple, small cervicomediastinal cystic hygromas occurring in an asymptomatic 43-year-old woman with no history of trauma, thoracic surgery, malignancy, infection or tuberculosis. Echocardiography showed a large amount of pericardial effusions and pericardial fluid analysis revealed inappropriately elevated triglyceride. We did not demonstrate communication between the thoracic duct and the pericardial sac by lymphangiography and chest computed tomography. She successfully responded to 30 days of continuous pericardial drainage and 15 days of a medium-chain triglyceride diet after 30 days of total parenteral nutrition. Follow-up echocardiography 6 months after treatment commencement showed a minimal reaccumulation of pericardial fluid without symptom. We conclude that if a patient is asymptomatic and can well tolerate daily life, surgery including pericardiectomy or ligation of the thoracic duct is not necessarily required.
Adult
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Female
;
Humans
;
Lymphangioma, Cystic/*complications/pathology
;
Mediastinal Cyst/*complications/pathology
;
Neck/pathology
;
Pericardial Effusion/*etiology/pathology/therapy
3.The fate of traumatic subdural hygroma in serial computed tomographic scans.
Kyeong Sook LEE ; Won Kyoung BAE ; Hack Gun BAE ; Il Gyu YUN
Journal of Korean Medical Science 2000;15(5):560-568
We reviewed serial computed tomographic (CT) scans of 58 patients with traumatic subdural hygroma (SDG) to investigate its natural history. All were re-evaluated with a special reference to the size and density of SDG. Thirty-four patients (58.6%) were managed conservatively and 24 patients (41.4%) underwent surgery. The lesion was described as remained, reduced, resolved, enlarged and changed. Means of interval from injury to diagnosis and any changes in CT were calculated. SDGs were resolved in 12 (20.7%), reduced in 15 (25.9%), remained in 10 (17.2%), enlarged in 2 (3.4%), and changed into chronic subdural hematoma (CSDH) in 19 patients (32.8%). SDG was diagnosed at 11.6 days after the injury. It was enlarged at 25.5 days, remained at 46.0 days, reduced at 59.3 days, resolved at 107.5 days, and changed into CSDH at 101.5 days in average. SDGs were developed as delayed lesions, and changed sequentially. They enlarged for a while, then reduced in size. The final path of a SDG was either resolution or CSDH formation. Nearly half of SDGs was resolved or reduced within three months, however, 61.3% of unresolved or unreduced SDG became iso- or hyperdense CSDH. These results suggest that the unresolved SDG is the precursor of CSDH.
Adolescence
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Adult
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Aged
;
Aged, 80 and over
;
Child
;
Child, Preschool
;
Craniocerebral Trauma/complications
;
Disease Progression
;
Hematoma, Subdural, Chronic/radiography*
;
Hematoma, Subdural, Chronic/pathology*
;
Hematoma, Subdural, Chronic/etiology
;
Human
;
Infant
;
Longitudinal Studies
;
Lymphangioma/radiography
;
Lymphangioma/pathology
;
Lymphangioma/etiology
;
Middle Age
;
Subdural Effusion/radiography*
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Subdural Effusion/pathology*
;
Subdural Effusion/etiology
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Tomography, X-Ray Computed*
4.Submucosal lymphatic cyst of the stomach.
Young Jun KIM ; Kyung Sup CHUNG ; Jae Bock CHUNG ; Sang In LEE ; In Suh PARK ; Heung Jae CHOI ; Kyung Sik LEE ; Nam Hoon CHO ; Chan Il PARK
Yonsei Medical Journal 1989;30(4):387-391
A submucosal lymphatic cyst is a thin-walled cyst, lined by flattened lymphatic endothelium, containing thin serous fluid. It rarely causes clinical symptoms, and it is incidentally discovered during fiberoptic panendoscopy or radiologic study in most cases. It is an extremely rare benign tumor of the stomach; however, a submucosal lymphatic cyst should be considered if a pliable and benign submucosal lesion is detected during fiberoptic panendoscopy. We report a case of submucosal lymphatic cyst of the stomach which showed a typical clinical picture. This report is the first case of submucosal lymphatic cyst of the stomach in Korea to the best of our knowledge.
Age Factors
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Biopsy
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Case Report
;
Gastric Mucosa/pathology
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Human
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Lymphangioma/etiology/*pathology/surgery
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Male
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Middle Age
;
Stomach Neoplasms/etiology/*pathology/surgery
5.Submucosal lymphatic cyst of the stomach.
Young Jun KIM ; Kyung Sup CHUNG ; Jae Bock CHUNG ; Sang In LEE ; In Suh PARK ; Heung Jae CHOI ; Kyung Sik LEE ; Nam Hoon CHO ; Chan Il PARK
Yonsei Medical Journal 1989;30(4):387-391
A submucosal lymphatic cyst is a thin-walled cyst, lined by flattened lymphatic endothelium, containing thin serous fluid. It rarely causes clinical symptoms, and it is incidentally discovered during fiberoptic panendoscopy or radiologic study in most cases. It is an extremely rare benign tumor of the stomach; however, a submucosal lymphatic cyst should be considered if a pliable and benign submucosal lesion is detected during fiberoptic panendoscopy. We report a case of submucosal lymphatic cyst of the stomach which showed a typical clinical picture. This report is the first case of submucosal lymphatic cyst of the stomach in Korea to the best of our knowledge.
Age Factors
;
Biopsy
;
Case Report
;
Gastric Mucosa/pathology
;
Human
;
Lymphangioma/etiology/*pathology/surgery
;
Male
;
Middle Age
;
Stomach Neoplasms/etiology/*pathology/surgery
6.Intussusception Secondary to Jejunal Lymphangioma in a 13-year-old Girl.
Ho Sung PARK ; Ho LEE ; Woo Sung MOON ; Seung Chan LEE ; Woo Bong CHOI ; Hyun Woong CHOI
The Korean Journal of Gastroenterology 2007;49(4):256-259
Lymphangioma is a benign tumor composed of numerous small or large thin-walled lymphatic spaces. It shows a predilection for head, neck, and axilla. Jejunal lymphangioma in children is extremely rare. We present a case of 13-year-old girl with jejuno-jejunal intussusception secondary to lymphangioma in jejunum. To our knowledge, this is the second report of jejunal lymphangioma causing intussusception in a child.
Adolescent
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Female
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Humans
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Intussusception/*etiology/surgery
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Jejunal Diseases/*etiology/surgery
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Jejunal Neoplasms/*complications/*diagnosis/pathology
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Lymphangioma/*complications/*diagnosis/pathology
;
Tomography, X-Ray Computed
8.Prognosis of fetuses with cystichygroma and nuchal translucency/nuchal fold thickening on prenatal echography.
Yayun WANG ; Yuan CHEN ; Mengmeng YANG ; Fangfang XI ; Qitao ZHAN ; Ying JIANG ; Baihui ZHAO ; Qiong LUO
Journal of Zhejiang University. Medical sciences 2019;48(4):434-438
OBJECTIVE:
To analyze the prognosis of fetuses with cystic hygroma (CH) or nuchal translucency (NT) or nuchal fold (NF) thickening detected by prenatal echography.
METHODS:
From January 2014 to December 2015, 124 fetuses with CH and NT/NF thickening on prenatal echography were enrolled from Women's Hospital of Zhejiang University School of Medicine. The basic clinical information, ultrasonic results, pregnancy outcomes and newborn follow-ups were analyzed. The cases were grouped by prognosis and the factors affecting prognosis were analyzed with logistic regression.
RESULTS:
There were 85 cases of labor induction including one stillbirth and 39 cases delivered. Except one infant who died after birth, all live births survived with good prognosis. Univariate analysis showed that the gestational age at diagnosis of poor prognosis group was earlier than that of good prognosis group (<0.01); and the former group also had higher hydrops fetalis rate and additional structural anomalies rate (all <0.01). Multivariate regression analysis showed that hydrops fetalis (=90.105, <0.05) and additional structural anomalies (=61.854, <0.05) were risk factors of poor prognosis in fetuses with CH and NT/NF thickening.
CONCLUSIONS
Fetuses with diagnosed CH or NT/NF thickening on prenatal ultrasonography are likely to be associated with chromosomal abnormality. Early gestational weeks, hydrops fetalis and additional structural anomalies may indicate poor prognosis.
Female
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Fetus
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Humans
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Hydrops Fetalis
;
etiology
;
Infant, Newborn
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Lymphangioma, Cystic
;
complications
;
diagnosis
;
Nuchal Translucency Measurement
;
Pregnancy
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Pregnancy Outcome
;
Prognosis
;
Ultrasonography, Prenatal
9.Small Bowel Volvulus Induced by Mesenteric Lymphangioma in an Adult: a Case Report.
Jin Hee JANG ; Su Lim LEE ; Young Mi KU ; Chang Hyeok AN ; Eun Deok CHANG
Korean Journal of Radiology 2009;10(3):319-322
Mesenteric lymphangiomas are rare abdominal masses that are seldom associated with small bowel volvulus, and especially in adult patients. We report here on an unusual case of small bowel volvulus that was induced by a mesenteric lymphangioma in a 43-year-old man who suffered from repeated bouts of abdominal pain. At multidetector CT, we noticed whirling of the cystic mesenteric mass and the adjacent small bowel around the superior mesenteric artery. Small bowel volvulus induced by the rotation of the mesenteric lymphangioma was found on exploratory laparotomy. Lymphangioma should be considered as a rare cause of small bowel volvulus in adult patients.
Abdominal Pain/etiology
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Adult
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Contrast Media/diagnostic use
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Diagnosis, Differential
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Humans
;
Intestinal Volvulus/*diagnosis/etiology/surgery
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Intestine, Small/*radiography/surgery
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Lymphangioma/*complications/surgery
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Male
;
Mesenteric Artery, Superior/*radiography/surgery
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Radiographic Image Enhancement/methods
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Rare Diseases
;
Tomography, X-Ray Computed
10.A Case of Cardiac Lymphangioma Presenting as a Cystic Mass in the Right Atrium.
Shin Jae KIM ; Eun Seok SHIN ; Seon Woon KIM ; Je Kyoun SHIN ; Jong Pil CHEONG ; Young Min KIM ; Sang Gon LEE
Yonsei Medical Journal 2007;48(6):1043-1047
A 44-year-old woman underwent surgery for an asymptomatic primary tumor of the heart located in the right atrium. The tumor was detected incidentally during follow-up computed tomography for a resected breast cancer. The mass, lying along the lower portion of the right atrial septum, was homogenous and cystic in nature, as detected by transthoracic and transesophageal echocardiography. Complete resection was performed via a median sternotomy under cardiopulmonary bypass. The postoperative course was uneventful. However, the histological result was surprising: the mass was a cardiac lymphangioma.
Adult
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Breast Neoplasms/complications/pathology
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Cysts/etiology/pathology
;
Echocardiography, Transesophageal
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Female
;
Heart Atria
;
Heart Neoplasms/complications/*diagnosis/surgery
;
Humans
;
Lymphangioma/complications/*diagnosis/surgery
;
Myocardium/*pathology
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Tomography, X-Ray Computed