Results 141 to 150 of about 4,369 (185)
Thoracic Lymphangiomatosis in a Child
Journal of Pediatric Hematology/Oncology, 2004 An 8-year-old boy who presented with a mediastinal mass, pulmonary infiltrates, and disseminated intravascular coagulation was diagnosed with lymphangiomatosis. Despite medical management, he developed multiple organ failure and died. The authors discuss the diagnostic findings, medical management, and pathology and review 52 additional cases of ...
Ofelia A, Alvarez +2 more
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Diffuse Lymphangiomatosis of Bone
Journal of Medical Imaging and Radiation Oncology, 1999Two cases of lymphangiomatosis of bone, a very rare systemic condition characterized by both skeletal and parenchymal lesions, are presented. The skeletal changes have an appearance similar to haemangiomas in the spine, and soap-bubbly lesions in the flat bones. One case carried the diagnosis of eosinophilic granuloma for 18 years. The findings on MRI,
Harry J Griffiths +2 more
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Lymphangiomatosis of the Ileum With Perforation: A Case Report and Review of the Literature [PDF]
Annals of Medicine and Surgery, 2019 Lymphangiomatosis is a benign proliferation of lymph vessels. Lymphatic diseases can vary from small lymphangioma to generalized lymphangiomatosis, which is a rare condition and can have several clinical manifestations.
Mario Schietroma +2 more
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Splenic Lymphangiomatosis Showing Rapid Growth During Lactation: A Case Report [PDF]
World Journal of Gastroenterology, 2010 Splenic lymphangiomatosis is a very rare condition that, from 1990 to date, has been described only nine times. In the present report, we describe the first case of splenic lymphangiomatosis with rapid growth during lactation in a 35-year-old woman.
Rosalia Patti
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Radiology, 1969
Solitary Hemangioma of bone and the more recently accepted dysplastic disorder of hemangiomatosis, which may lead to “vanishing bones,” are established clinical, pathological, and radiological entities. Much less commonly described are the lymphangiomatous counterparts, solitary lymphangioma and generalized lymphangiomatosis.
G M, Steiner, J, Farman, J P, Lawson
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Solitary Hemangioma of bone and the more recently accepted dysplastic disorder of hemangiomatosis, which may lead to “vanishing bones,” are established clinical, pathological, and radiological entities. Much less commonly described are the lymphangiomatous counterparts, solitary lymphangioma and generalized lymphangiomatosis.
G M, Steiner, J, Farman, J P, Lawson
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Lymphangiomatosis with Dental Involvement
Lymphatic Research and Biology, 2015Lymphangiomatosis characterized by lymphangiomatous proliferation is a rare disease of unknown etiology, which seems to be more aggressive than Gorham-Stout Syndrome, also known as "the vanished bone disease."A woman presented with a lytic lesion in the tibia and multiple lytic lesions in teeth dentin.
Mordechai, Findler +2 more
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Hindquarter amputation for lymphangiomatosis
European Journal of Surgical Oncology (EJSO), 1996We describe the presentation of a 16-year-old boy with locally advanced lymphangiomatosis affecting the left thigh and groin. This is a difficult disease to both diagnose and treat, and one in which radical surgery may be necessary to effect a cure or even palliation.
M P, Jenkins, I J, Laidlaw, J M, Thomas
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Lymphoscintigraphy in the Diagnosis of Lymphangiomatosis
Clinical Nuclear Medicine, 2010Lymphangiomatosis is a rare condition characterized by multiple abnormalities of the lymphatic system. Diagnosis is often difficult, as chronic, intermittent, or acute pain; edema; and other symptoms may affect the respiratory, gastrointestinal, renal, hepatic, skeletal, and other organ systems.
Nicole, Beveridge +2 more
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Radiology, 2008
A 37-year-old healthy female nonsmoker presented with hemoptysis. Her medical history was remarkable for sickle cell trait and iron deficiency anemia. She had not traveled outside North America. Computed tomography (CT) and magnetic resonance (MR) imaging were performed in the chest and abdomen.
Prachi P, Agarwal +2 more
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A 37-year-old healthy female nonsmoker presented with hemoptysis. Her medical history was remarkable for sickle cell trait and iron deficiency anemia. She had not traveled outside North America. Computed tomography (CT) and magnetic resonance (MR) imaging were performed in the chest and abdomen.
Prachi P, Agarwal +2 more
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Lymphangiomatosis: A Case Report
Southern Medical Journal, 2005Lymphangiomatosis is a rare congenital malformation that can involve visceral organs, soft tissue, and bone. This report describes a 5-year-old female with this disorder who presented with respiratory distress and subsequently died. Clinical, diagnostic, and treatment aspects of this entity are discussed.
Dan, Tran +2 more
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