1.A Rare Case of Diffuse Pulmonary Lymphangiomatosis in a Middle-Aged Woman.
Hyun Ju LIM ; Joungho HAN ; Hong Kwan KIM ; Tae Sung KIM
Korean Journal of Radiology 2014;15(2):295-299
Diffuse pulmonary lymphangiomatosis (DPL) is a rare lymphatic disorder characterized by lymphatic channel proliferation. It is mostly reported in children and young adults. Here, we report a case involving a 52-year-old asymptomatic woman who presented with increased interstitial markings, as seen on a chest radiograph. Diffuse interstitial septal thickening was found on a serial follow-up chest computed tomography scan, and lymphangitic metastasis was the primary radiologic differential diagnosis. However, histologic sections of wedge resected lung revealed diffuse pleural and interlobular septal lymphatic proliferation characteristic of DPL.
Diagnosis, Differential
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Female
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Humans
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Lung Neoplasms/pathology/*radiography
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Lymphangioma/pathology/*radiography
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Middle Aged
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Rare Diseases/pathology/*radiography
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Tomography, X-Ray Computed
2.A Case of Isolated Hepatic Lymphangioma.
Seol Jung AK ; Seung Keun PARK ; Hee Ug PARK
The Korean Journal of Gastroenterology 2012;59(2):189-192
Hepatic lymphangioma is a rare benign neoplasm. It usually occurs as a part of systemic lymphangiomatosis. Isolated hepatic lymphangioma is extremely rare. A 58-year-old woman with weight loss was referred for the evaluation of chronic renal insufficiency and hepatic mass. Abdominal computed tomography showed 3 cm sized multilobulated cystic lesion with calcification and thick septal enhancing focus in the segment V of the liver. On abdominal magnetic resonance imaging, the masses exhibited low signal intensity on the T1-weighted images and high signal intensity on the T2-weighted images. Malignant tumor could not be ruled out, and therefore, the patient underwent right anterior segmentectomy of the liver. Gross pathology reveraled a 3.0x2.2x1.5 cm mass with multichamber cyst, which was filled with mucoid material. Histologically the mass was composed of irregularly shaped vascular channels filled acellular homogeneous lymph fluids. The final diagnosis was hepatic isolated cavernous lymphangioma. Herein, we report a case of isolated hepatic lymphangioma and also review the existing literature.
Female
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Humans
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Liver Diseases/*diagnosis/pathology/radiography
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Lymphangioma/*diagnosis/pathology/radiography
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Middle Aged
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Renal Insufficiency, Chronic/diagnosis
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Tomography, X-Ray Computed