Lymphangioma - لِففنگوئما
لِففنگوئما (Lymphangioma) ليمفيٽڪ سسٽم جون خرابيون آهن جن کي زخمن سان منسوب ڪيو ويو آهي جيڪي پتلي ڀت وارا سيسٽ آهن. اهي خرابيون ڪنهن به عمر ۾ ٿي سگهن ٿيون ۽ جسم جي ڪنهن به حصي ۾ شامل ٿي سگهن ٿيون، پر 90٪ 2 سالن کان گهٽ عمر وارن ٻارن ۾ ٿينديون آهن ۽ انهن ۾ مٿي ۽ ڳچيءَ ۾ شامل هوندا آهن. لمفنگيوماس عام طور تي جنين جي الٽراسونوگرافي ذريعي پيدائش کان اڳ تشخيص ڪيا ويندا آهن. حاصل ڪيل lymphangiomas شايد سورن، سوزش، يا لففيڪ رڪاوٽ جي نتيجي ۾. جيئن ته انهن کي خراب ٿيڻ جو ڪو به موقعو نه آهي، lymphangiomas عام طور تي صرف کاسمیٹڪ سببن لاء علاج ڪيو ويندو آهي.
☆ 2022 ۾ جرمني مان Stiftung Warentest نتيجن، ModelDerm سان صارفين جي اطمينان صرف ادا ڪيل ٽيلي ميڊيسن مشوري جي ڀيٽ ۾ ٿورو گهٽ هئي.
References
Lymphangioma lymphatic malformation (LM) جي نالي سان پڻ سڃاتو وڃي ٿو. اهو پيدائش کان موجود هڪ ويسولر خرابي آهي. اهو ڄمڻ کان اڳ ۽ بعد ۾ لففيڪ ٽائيس جي غير معمولي واڌ جي خاصيت آهي. Lymphangioma 2000 کان 4000 ماڻهن ۾ اٽڪل 1 کي متاثر ڪري ٿو، جن ۾ جنس يا نسل جي وچ ۾ ڪو خاص فرق ناهي. اڪثر ڪيس (80-90٪) ٻن سالن کان اڳ تشخيص ڪيا ويا آهن. علامتون وڏي پئماني تي مختلف ٿين ٿيون، مقامي سطح تي سوجن کان وٺي لففيڪ چينلز ۾ وسيع غيرمعموليات تائين، ڪڏهن ڪڏهن سخت سوز جو سبب بڻجي ٿو جنهن کي elephantiasis طور سڃاتو وڃي ٿو. مثال طور، ڳچيء ۽ منهن ۾ lymphangioma منهن جي سوز جو سبب بڻجي سگهي ٿو، ۽ سخت ڪيسن ۾، بگڙيل. جڏهن اهو زبان تي اثر انداز ٿئي ٿو، اهو جبڑے جي واڌ ۽ غلط دانت جي ڪري سگھي ٿو. وات ۽ ڳچيء ۾، اهو سانس جي مشڪلاتن ۽ زندگي جي خطري واري بيماري پيدا ڪري سگهي ٿي. اکين ۾، اهو ٿي سگهي ٿو بصارت جي نقصان، اکين جي محدود حرڪت، ٻرندڙ پلڪون، ۽ اکيون ٻرندڙ. عضون جي شموليت سبب ٿي سگهي ٿي سوز ۽ غير معمولي واڌ ۽ نسب ۽ هڏا. هي طومار عام طور تي سست وڌندو آهي، پر انفيڪشن، هارمونل تبديليون، يا زخم تيزيءَ سان ترقي ڪري سگهن ٿا، زندگيءَ لاءِ خطرو پيدا ڪري سگهن ٿا جن کي فوري علاج جي ضرورت آهي.
Lymphangioma (lymphatic malformation, LM), a congenital vascular disease, is a low-flow vascular abnormality in lymphatic diseases that is characterized by excessive growth of lymphatic tissue during prenatal and postpartum development. The incidence rate of LM is ~1:2000–4000, with no variation between genders and races. Most patients (80–90%) are diagnosed before the age of two. The clinical manifestations of lymphangioma are quite different among patients, varying from local swelling leading to superficial mass to a large area of diffuse infiltrating lymphatic channel abnormalities resulting in elephantiasis. Cervicofacial LM can cause facial elephantiasis, and in some severe cases, it can lead to serious disfigurement of the face. Tongue LM can lead to mandibular overgrowth and occlusal asymmetry, and oral and cervical LM can cause obstructive acute respiratory distress and life-threatening situations. Orbital LM may lead to decreased vision, decreased extraocular muscle movement, ptosis and exophthalmos. LM of the extremities can trigger swelling or gigantism, accompanied by overgrowth of soft tissue and bones. LM usually grows slowly and steadily, but under certain conditions, such as infection, hormonal changes or trauma, it can grow explosively and become a life-threatening disease requiring immediate treatment.
Lymphangioma (lymphatic malformation, LM), a congenital vascular disease, is a low-flow vascular abnormality in lymphatic diseases that is characterized by excessive growth of lymphatic tissue during prenatal and postpartum development. The incidence rate of LM is ~1:2000–4000, with no variation between genders and races. Most patients (80–90%) are diagnosed before the age of two. The clinical manifestations of lymphangioma are quite different among patients, varying from local swelling leading to superficial mass to a large area of diffuse infiltrating lymphatic channel abnormalities resulting in elephantiasis. Cervicofacial LM can cause facial elephantiasis, and in some severe cases, it can lead to serious disfigurement of the face. Tongue LM can lead to mandibular overgrowth and occlusal asymmetry, and oral and cervical LM can cause obstructive acute respiratory distress and life-threatening situations. Orbital LM may lead to decreased vision, decreased extraocular muscle movement, ptosis and exophthalmos. LM of the extremities can trigger swelling or gigantism, accompanied by overgrowth of soft tissue and bones. LM usually grows slowly and steadily, but under certain conditions, such as infection, hormonal changes or trauma, it can grow explosively and become a life-threatening disease requiring immediate treatment.
هن پٺتي پيل مطالعي ۾، اسان 24 ٻارن جو جائزو ورتو جن جو lymphangioma هو ۽ جن جو جنوري 1999 کان ڊسمبر 2004 تائين بليومائسن محلول جي انجيڪشن سان علاج ڪيو ويو. اڪثر زخم (63٪) مڪمل طور تي ختم ٿي ويا، 21٪ سٺو جواب مليو، ۽ 16٪ سٺو جواب نه ڏنو. ٻن مريضن کي ٽيومر بعد ۾ واپس آيو، ۽ ٻن ٻين کي ڦڦڙن جو شڪار ٿيو جتي انهن کي انجيڪشن لڳايا ويا. خوشقسمتيءَ سان، اسان ڪو ٻيو وڏو مسئلو يا ضمني اثرات نه ڏٺا.
This is a retrospective study of 24 children diagnosed with lymphangioma and treated with intralesional injection of bleomycin aqueous solution from January 1999 to December 2004. Complete resolution was seen in 63% (15/24) of lesions, 21% (5/24) had good response and 16% (4/24) had poor response. The tumour recurred in 2 patients. Two other patients had abscess formation at the site of injection. No other serious complications or side effects were observed.
This is a retrospective study of 24 children diagnosed with lymphangioma and treated with intralesional injection of bleomycin aqueous solution from January 1999 to December 2004. Complete resolution was seen in 63% (15/24) of lesions, 21% (5/24) had good response and 16% (4/24) had poor response. The tumour recurred in 2 patients. Two other patients had abscess formation at the site of injection. No other serious complications or side effects were observed.
Lymphangioma جا مکيه قسم هن ريت آهن - lymphangioma circumscriptum, cavernous lymphangioma, cystic hygroma, lymphangioendothelioma. اهي لڳ ڀڳ 26 سيڪڙو بنائنائن ويسڪولر ٽومر ٻارن ۾ ٿين ٿا پر بالغن ۾ گهٽ عام آهن. Lymphangioma circumscriptum ، سڀ کان وڌيڪ اڪثر قسم، ڏيکاري ٿو لففيڪ نلڪن کي چمڙي جي ذريعي نڪرندي، صاف رطوبت سان ڀريل ويسيڪلز جهڙوڪ ڏيڏر جي اسپون وانگر، ٽشو جي سوجن سان گڏ. اهو عام طور تي انهن علائقن تي ظاهر ٿئي ٿو جن ۾ هڪ امير لففيڪ نيٽ ورڪ جهڙوڪ ٽنگ، ٽرن، ۽ بغل. اسان جي ڪلينڪ تي هڪ 71 سالن جي عورت آئي، جنهن ۾ پيرن جي مسلسل سوڄ هئي، هن جي جينات تي گلابي ڌڪ، خارش ۽ لفف فلوئڊ نڪرندي هئي. اسان جراحتي طريقي سان سڀني bumps کي هٽائي ڇڏيو جنهن کي bilateral major labiectomy سڏيو ويندو آهي، کولس جي فاشيا جي سطح تي روڪيندي، ڪلائيٽرس ۽ چارچٽ کي محفوظ ڪندي.
The predominant types of lymphangioma are lymphangioma circumscriptum (LC), cavernous lymphangioma, cystic hygroma, and lymphangioendothelioma. These entities account for approximately 26% of benign vascular tumors in children but are rarer in adults. LC is the most common form of cutaneous lymphangioma and is characterized by superficial lymphatic ducts protruding through the epidermis. This condition results in clusters of clear fluid-filled vesicles resembling frog spawn and associated tissue edema. It is usually found on the proximal extremity, trunk, and axilla, which has an abundant lymphatic system. A 71-year-old female presented to our outpatient clinic with persistent edema of both lower limbs, clusters of pink labial papules, pruritus, and watery lymph oozing. We removed all the papules by performing bilateral major labiectomy down to the level of Colles' fascia, sparing the clitoris and fourchette.
The predominant types of lymphangioma are lymphangioma circumscriptum (LC), cavernous lymphangioma, cystic hygroma, and lymphangioendothelioma. These entities account for approximately 26% of benign vascular tumors in children but are rarer in adults. LC is the most common form of cutaneous lymphangioma and is characterized by superficial lymphatic ducts protruding through the epidermis. This condition results in clusters of clear fluid-filled vesicles resembling frog spawn and associated tissue edema. It is usually found on the proximal extremity, trunk, and axilla, which has an abundant lymphatic system. A 71-year-old female presented to our outpatient clinic with persistent edema of both lower limbs, clusters of pink labial papules, pruritus, and watery lymph oozing. We removed all the papules by performing bilateral major labiectomy down to the level of Colles' fascia, sparing the clitoris and fourchette.
