Lymphangioma
Lymphangioma ແມ່ນຄວາມຜິດປົກກະຕິຂອງລະບົບ lymphatic ທີ່ມີລັກສະນະແບບບາດແຜທີ່ມີຝາບາງໆ. ຄວາມຜິດປົກກະຕິເຫຼົ່ານີ້ສາມາດເກີດຂຶ້ນໃນທຸກຄົນ ແລະທຸກອາຍຸ, ແຕ່ 90% ເກີດຂຶ້ນໃນເດັກທີ່ມີອາຍຸຕ່ຳກວ່າ 2 ປີ ແລະກ່ຽວຂ້ອງກັບຫົວ ແລະຄໍ. Lymphangiomas ແມ່ນຖືກວິນິດໄສກ່ອນການເກີດໂດຍໃຊ້ ultrasound fetal. lymphangiomas ທີ່ໄດ້ຮັບອາດຈະເປັນຜົນມາຈາກການບາດເຈັບ, ການອັກເສບ ຫຼືການອຸດຕັນຂອງ lymphatic. ເນື່ອງຈາກພວກເຂົາບໍ່ມີໂອກາດທີ່ຈະເປັນໂຣກຮ້າຍ, lymphangiomas ມັກຈະຖືກປິ່ນປົວໂດຍສາເຫດຜົນດ້ານອຸບາຍພຽງແຕ່.
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ໃນປີ 2022 Stiftung Warentest ຜົນໄດ້ຮັບຈາກເຢຍລະມັນ, ຄວາມພໍໃຈຂອງຜູ້ບໍລິໂພກກັບ ModelDerm ແມ່ນຕໍ່າກວ່າການປຶກສາຫາລືທາງດ້ານການປິ່ນປົວທາງໂທລະສັບເລັກນ້ອຍເທົ່ານັ້ນ.
ໃນປີ 2022 Stiftung Warentest ຜົນໄດ້ຮັບຈາກເຢຍລະມັນ, ຄວາມພໍໃຈຂອງຜູ້ບໍລິໂພກກັບ ModelDerm ແມ່ນຕໍ່າກວ່າການປຶກສາຫາລືທາງດ້ານການປິ່ນປົວທາງໂທລະສັບເລັກນ້ອຍເທົ່ານັ້ນ.
relevance score : -100.0%
ReferencesLymphangioma ແມ່ນພະຍາດທີ່ຮູ້ຈັກວ່າ lymphatic malformation (LM). ມັນເປັນການຜິດປົກກະຕິຂອງສະແດງຂອງລິມຟັດທີ່ກໍ່ຕັ້ງຂຶ້ນຈາກການກໍ່ຕັ້ງຂອງສະແດງລິມຟັດ. ມັນສະແດງອອກດ້ວຍການຂະຫຍາຍຂອງສະແດງລິມຟັດທີ່ກ່ອນ ແລະ ຫຼັງການກໍ່ຕັ້ງ. Lymphangioma ມີອັດຕາການເກີດປະມານ 1 ໃນ 2,000‑4,000 ຄົນ, ແບບບໍ່ແຕກຕ່າງຕາມ ເພດ ຫຼື ຊາດ. ສ່ວນໃຫຍ່ (80‑90 %) ຂອງກໍລະນີຖືກກວດພົບໃນອາຍຸກ່ອນ 2 ປີ. ອາການຂອງ lymphangioma ສາມາດແກ່ຕັ້ງແຕ່ການເກັບຊັບໃນຜິວດິນ, ການຂະຫຍາຍໃນທາງລິມຟັດທົ່ວໂລກ, ຫຼື ການກໍ່ຕັ້ງຊັບຊ່ວຍທີ່ຮູ້ຈັກວ່າ “ພະຍາດຊ້າງ”. ຕົວຢ່າງ, lymphangioma ຢູ່ຄໍ ຫຼື ບໍລິສັດຜິວສາມາດເຮັດໃຫ້ເກີດການເກັບຊັບຂອງຜິວ, ແລະ ໃນກໍລະນີຮ້າຍແຮງ ການຜິດປົກກະຕິກໍ່ສາມາດເກີດຂຶ້ນ. ເມື່ອມັນກະທົບຕໍ່ຕາຍ, ມັນອາດເຮັດໃຫ້ມີການຂະຫຍາຍຂອງຕາດ້ານກາງ ແລະ ການສ້າງຂອງຕາທີ່ບໍ່ຖືກຕ້ອງ. ໃນປາກ ແລະ ຄໍ, lymphangioma ອາດເຮັດໃຫ້ເກີດການສູນເສຍສັດຕິດ, ການສູນເສຍຊີວິດ ຫຼື ການສູນເສຍສັດຕິດທີ່ສໍາພັນກັບຊີວິດ. ໃນຕາ, ມັນອາດເຮັດໃຫ້ມີການສູນເສຍການເບິ່ງເຫັນ, ການເຄື່ອນໄຫວຂອງຕາຈຳກັດ, ຕາປຸນ ຫຼື ຕາປູນລົດລົງ. ການມີສ່ວນຮ່ວມຂອງແຂນຂາສາມາດເຮັດໃຫ້ເກີດການເກັບຊັບ ແລະ ການຂະຫຍາຍຂອງສະແດງລິມຟັດ ແລະ ການກໍ່ຕັ້ງກັບການກະດູກ. ອັດຕະລັດອອກຈາກການກໍ່ຕັ້ງອາດຈະເຕີບໂຕຊ້າ, ແຕ່ການຕິດເຊື່ອງ, ການປ່ຽນແປງຂອງຮໍ່ຮອຍ ຫຼື ການບາດເຈັບສາມາດເຮັດໃຫ້ການຂະຫຍາຍແບບໄວແລະມີຄວາມສ່ຽງຕໍ່ຊີວິດທີ່ຕ້ອງການການປິ່ນປົວດ່ວນ.
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.
ໃນການສຶກສານີ້, ພວກເຮົາໄດ້ທົບທວນກັບເດັກນ້ອຍ 24 ຄົນທີ່ມີ lymphangioma ແລະໄດ້ຮັບການປິ່ນປົວດ້ວຍຢາ bleomycin ຕັ້ງແຕ່ເດືອນມັງກອນ 1999 ຫາເດືອນທັນວາ 2004. ສ່ວນໃຫຍ່ຂອງບາດແຜ (63%) ຫາຍໄປຫມົດ, 21% ມີການຕອບສະໜອງດີ, ແລະ 16% ບໍ່ຕອບສະໜອງດີ. ສອງຄົນມີເນື້ອງອກກັບຄືນໃນເວລາຕໍ່ມາ, ແລະອີກ 2 ຄົນເປັນຝີບ່ອນທີ່ພວກເຂົາໄດ້ຮັບການສັກຢາ. ໂຊກດີ, ພວກເຮົາບໍ່ເຫັນບັນຫາໃຫຍ່ ຫຼືຜົນຂ້າງຄຽງອື່ນໆ.
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.
ປະເພດຕົ້ນຕໍ່ຂອງ lymphangioma ມີດັ່ງນີ້ — lymphangioma circumscriptum, cavernous lymphangioma, cystic hygroma, lymphangioendothelioma. ເຫຼົ່ານີ້ປະກອບປະມານ 26% ຂອງເນື້ອງອກ vascular benign ໃນເດັກນ້ອຍ, ແຕ່ບໍ່ຄ່ອຍພົບໃນຜູ້ໃຫຍ່. Lymphangioma circumscriptum ແມ່ນປະເພດທີ່ພົບເລິກທີ່ສຸດ, ສະແດງໃຫ້ເຫັນທໍ່ lymphatic protrusion ຜ່ານຜິວຫນັງ, ປະກອບເປັນ vesicles ທີ່ມີນ້ຳ ແລະ ຈະແຈ້ງຄ້າຍກັບການວາງໄຂ່ຂອງກົບ, ຄຽງຄູ່ກັບການໃຄ່ບວມຂອງເນື້ອເຍື່ອ. ດ້ວຍປົກກະຕິ, ມັນປາກົດຢູ່ໃນພື້ນທີ່ທີ່ມີຕາຫນ່າງ lymphatic ອຸດົມສົມບູນເຊັ່ນ ແຂນຂາ, ລໍາຕົ້ນ, ແລະ armpits. ຜູ້ຍິງອາຍຸ 71 ປີ ຄົນໜຶ່ງໄດ້ມາທີ່ຄລີນິກຂອງພວກເຮົາ ດ້ວຍອາການບວມຂາຢ່າງຕໍ່ເນື່ອງ, ມີຕຸ່ມສີບົວຢູ່ບໍລິເວນອະໄວຍະວະເພດ, ມີອາການຄັນ, ແລະນ້ຳ lymph ທີ່ຮົ່ວ. ພວກເຮົາໄດ້ຜ່າຕັດຕຸ່ມທັງໝົດອອກດ້ວຍຂັ້ນຕອນທີ່ເອີ້ນວ່າ ການຜ່າຕັດຂະໜາດສອງຝ່າຍ, ຢຸດຢູ່ທີ່ລະດັບ fascia Colles, ໃນຂະນະທີ່ປົກປັກຮັກສາ clitoris ແລະ 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.
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.
