"19491"^^ . . "Lymphangiomatosis ist ein seltener Krankheitszustand, der durch eine diffuse Wucherung von Lymphgef\u00E4\u00DFen charakterisiert ist. Dies kann interne Organe, Knochen, Weichgewebe und die Haut betreffen. Die st\u00E4rkste Verbreitung findet man bei Kindern und jungen Erwachsenen. Symptome und Heilungschancen variieren stark zwischen den Individuen und in Abh\u00E4ngigkeit von den betroffenen Organen. Auch wenn noch wenig \u00FCber die Ursachen bekannt ist, so wird vermutet, dass es sich um ein seltenes Fehlwachstum handelt, das in einer abnormalen Entwicklung des lymphatischen Systems resultiert. Der Name Lymphangiomatosis hat seinen Ursprung in den W\u00F6rtern lymph- (Beschreibung des lymphatischen Systems), -angio- (Gef\u00E4\u00DF), -oma- (Tumor bzw. Zyste), -tosis (Zustand). Andere Namen f\u00FCr diese oder \u00E4hnliche Krankheiten lauten: allgemeines Lymphangiom, systemische zystische Angiomatose, multiple Lymphangiectasias, allgemeine bzw. diffuse lymphatische Fehlbildung, allgemeine lymphatische Anomalie. Eine einzelne Ansammlung von Lymphgef\u00E4\u00DFen oder Zysten nennt man Lymphangiom. Lymphangiomatosis beschreibt F\u00E4lle, wo ein Lymphangiom nicht als singul\u00E4re Masse vorliegt, sondern wo die St\u00F6rung weitverbreitet oder an verschiedenen Stellen vorliegt (z. B. wenn verschiedene K\u00F6rperteile betroffen sind). Die allgemeine Lymphangiomatosis wurde erstmals 1828 beschrieben."@de . . . . "Lymphangiomatosis"@en . . "Lymphangiomatosis is a condition where a lymphangioma is not present in a single localised mass, but in a widespread or multifocal manner. It is a rare type of tumor which results from an abnormal development of the lymphatic system."@en . "1054039707"^^ . . . "LYMF"@en . "Lymphangiomatose"@fr . . . . "Lymphangiomatosis ist ein seltener Krankheitszustand, der durch eine diffuse Wucherung von Lymphgef\u00E4\u00DFen charakterisiert ist. Dies kann interne Organe, Knochen, Weichgewebe und die Haut betreffen. Die st\u00E4rkste Verbreitung findet man bei Kindern und jungen Erwachsenen. Symptome und Heilungschancen variieren stark zwischen den Individuen und in Abh\u00E4ngigkeit von den betroffenen Organen. Auch wenn noch wenig \u00FCber die Ursachen bekannt ist, so wird vermutet, dass es sich um ein seltenes Fehlwachstum handelt, das in einer abnormalen Entwicklung des lymphatischen Systems resultiert."@de . "La linfangiomatosi \u00E8 una malattia rara a carattere congenito. \u00C8 una patologia a carico dei vasi linfatici ed \u00E8 il risultato di un errore congenito a carico del sistema linfatico e che si sviluppa alla ventesima settimana di gestazione. Si evidenzia con vasi linfatici pi\u00F9 numerosi e pi\u00F9 grandi del normale con canali linfatici dalla parete sottile anormalmente interconnessi e dilatati. La malattia pu\u00F2 coinvolgere un solo organo, ma pi\u00F9 spesso \u00E8 multiorgano."@it . "Lymphangiomatosis"@en . "Linfangiomatosi"@it . . . "La lymphangiomatose est une maladie rare caract\u00E9ris\u00E9e par une prolif\u00E9ration diffuse des vaisseaux lymphatiques. Un lymphangiome est une masse anarchique de vaisseaux lymphatiques. Dans la lymphangiomatose, les lymphangiomes (ou kystes) sont multiples, et r\u00E9partis d'une mani\u00E8re g\u00E9n\u00E9ralis\u00E9e ou multifocale (c'est-\u00E0-dire impliquant plusieurs parties du corps). La lymphangiomatose r\u00E9sulte d'un d\u00E9veloppement anormal du syst\u00E8me lymphatique mais ses causes ne sont pas bien connues."@fr . . . "La linfangiomatosi \u00E8 una malattia rara a carattere congenito. \u00C8 una patologia a carico dei vasi linfatici ed \u00E8 il risultato di un errore congenito a carico del sistema linfatico e che si sviluppa alla ventesima settimana di gestazione. Si evidenzia con vasi linfatici pi\u00F9 numerosi e pi\u00F9 grandi del normale con canali linfatici dalla parete sottile anormalmente interconnessi e dilatati. La malattia pu\u00F2 coinvolgere un solo organo, ma pi\u00F9 spesso \u00E8 multiorgano."@it . . . "\u30EA\u30F3\u30D1\u7BA1\u816B\u75C7"@ja . . "\u0627\u0644\u0648\u0631\u0645 \u0627\u0644\u0648\u0639\u0627\u0626\u064A \u0627\u0644\u0644\u0645\u0641\u064A"@ar . . "Lymphangiomatosis"@de . . . . . . . . "Lymphangiomatosis is a condition where a lymphangioma is not present in a single localised mass, but in a widespread or multifocal manner. It is a rare type of tumor which results from an abnormal development of the lymphatic system. It is thought to be the result of congenital errors of lymphatic development occurring prior to the 20th week of gestation. Lymphangiomatosis is a condition marked by the presence of cysts that result from an increase both in the size and number of thin-walled lymphatic channels that are abnormally interconnected and dilated. 75% of cases involve multiple organs. It typically presents by age 20 and, although it is technically benign, these deranged lymphatics tend to invade surrounding tissues and cause problems due to invasion and/or compression of adjacent structures. The condition is most common in the bones and lungs and shares some characteristics with Gorham\u2019s disease. Up to 75% of patients with lymphangiomatosis have bone involvement, leading some to conclude that lymphangiomatosis and Gorham\u2019s disease should be considered as a spectrum of disease rather than separate diseases. When it occurs in the lungs, lymphangiomatosis has serious consequences and is most aggressive in the youngest children. When the condition extends into the chest it commonly results in the accumulation of chyle in the linings of the heart and/or lungs. Chyle is composed of lymph fluid and fats that are absorbed from the small intestine by specialized lymphatic vessels called lacteals during digestion. The accumulations are described based on location: chylothorax is chyle in the chest; chylopericardium is chyle trapped inside the sack surrounding the heart; chyloascites is chyle trapped in the linings of the abdomen and abdominal organs. The presence of chyle in these places accounts for many of the symptoms and complications associated with both lymphangiomatosis and Gorham\u2019s disease. The incidence of lymphangiomatosis is unknown and it is often misdiagnosed. It is separate and distinct from lymphangiectasis, lymphangioleiomyomatosis (LAM), pulmonary capillary hemangiomatosis, Kaposi\u2019s sarcoma, and kaposiform hemangioendothelioma. Its unusual nature makes lymphangiomatosis (and Gorham\u2019s disease) a diagnostic and therapeutic challenge. A multidisciplinary approach is generally necessary for optimal diagnosis and symptom management. The term literally means lymphatic system (lymph) vessel (angi) tumor or cyst (oma) condition (tosis)."@en . "7246362"^^ . . . . . . 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\u0648\u0639\u0627\u0626\u064A \u0644\u0645\u0641\u064A."@ar . "La lymphangiomatose est une maladie rare caract\u00E9ris\u00E9e par une prolif\u00E9ration diffuse des vaisseaux lymphatiques. Un lymphangiome est une masse anarchique de vaisseaux lymphatiques. Dans la lymphangiomatose, les lymphangiomes (ou kystes) sont multiples, et r\u00E9partis d'une mani\u00E8re g\u00E9n\u00E9ralis\u00E9e ou multifocale (c'est-\u00E0-dire impliquant plusieurs parties du corps). La lymphangiomatose r\u00E9sulte d'un d\u00E9veloppement anormal du syst\u00E8me lymphatique mais ses causes ne sont pas bien connues. La maladie peut affecter les organes internes, les os, les tissus mous et / ou la peau. Elle est plus fr\u00E9quente chez les enfants et les jeunes adultes. Les sympt\u00F4mes et le pronostic varient consid\u00E9rablement entre les individus et selon les organes concern\u00E9s. Le terme lymphangiomatose provient des mots \u00ABlymphe\u00BB (liquide biologique transport\u00E9 par le syst\u00E8me lymphatique), \u00ABangio\u00BB (concernant les vaisseaux), \u00ABoma\u00BB (tumeur ou kyste), \u00ABtose \u00BB(maladie)."@fr . 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"\u30EA\u30F3\u30D1\u7BA1\u816B\u75C7\uFF08\u308A\u3093\u3071\u304B\u3093\u3057\u3085\u3057\u3087\u3046\u3001Lymphanghiomatosis\u3001Generalized lymphatic anomaly\uFF09\u306F\u5168\u8EAB\u81D3\u5668\u306B\u30EA\u30F3\u30D1\u7BA1\u7D44\u7E54\u304C\u5897\u6B96\u3059\u308B\u539F\u56E0\u4E0D\u660E\u306E\u5E0C\u5C11\u6027\u96E3\u6CBB\u6027\u75BE\u60A3\u3067\u3042\u308B\u3002\u5C0F\u5150\u3001\u82E5\u5E74\u8005\u306B\u591A\u304F\u767A\u75C7\u3057\u3001\u75C7\u72B6\u306F\u6D78\u6F64\u81D3\u5668\u306B\u3088\u308A\u69D8\u3005\u3060\u304C\u3001\u4E73\u3073\u80F8\u306A\u3069\u80F8\u90E8\u75C5\u5909\u3092\u5408\u4F75\u3059\u308B\u5834\u5408\u304C\u3042\u308B\u3002\u9AA8\u6EB6\u89E3\u3084\u4E73\u3073\u8179\u6C34\u3001\u813E\u81D3\u6D78\u6F64\u3001\u30EA\u30F3\u30D1\u6D6E\u816B\u3001\u8840\u6DB2\u51DD\u56FA\u7570\u5E38\u3082\u8D77\u3053\u3059\u3002 \u306A\u304A\u3001\u3053\u306E\u75BE\u60A3\u306E\u5C02\u9580\u7684\u306A\u60C5\u5831\u306F\u533B\u5E2B\u304C\u63D0\u4F9B\u3059\u308B\u300C\u30EA\u30F3\u30D1\u7BA1\u75BE\u60A3\u60C5\u5831\u30B9\u30C6\u30FC\u30B7\u30E7\u30F3\u300D\uFF08\u672B\u5DFB\u306B\u30EA\u30F3\u30AF\u3042\u308A\uFF09\u3092\u53C2\u7167\u3059\u308B\u3079\u304D\u3067\u3042\u308B\u3002"@ja . "Lung biopsy showing infiltration of lymphatic tissue."@en . "Lymphangiomatosis"@en .