Juvenile xanthogranuloma
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ໃນປີ 2022 Stiftung Warentest ຜົນໄດ້ຮັບຈາກເຢຍລະມັນ, ຄວາມພໍໃຈຂອງຜູ້ບໍລິໂພກກັບ ModelDerm ແມ່ນຕໍ່າກວ່າການປຶກສາຫາລືທາງດ້ານການປິ່ນປົວທາງໂທລະສັບເລັກນ້ອຍເທົ່ານັ້ນ.
ໃນປີ 2022 Stiftung Warentest ຜົນໄດ້ຮັບຈາກເຢຍລະມັນ, ຄວາມພໍໃຈຂອງຜູ້ບໍລິໂພກກັບ ModelDerm ແມ່ນຕໍ່າກວ່າການປຶກສາຫາລືທາງດ້ານການປິ່ນປົວທາງໂທລະສັບເລັກນ້ອຍເທົ່ານັ້ນ.
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ReferencesJuvenile xanthogranuloma (JXG) ເປັນເງື່ອນໄຂທີ່ພົບເລື້ອຍແລະເປັນປະເພດ non‑Langerhans cell histiocytic disorder ທີ່ສຸດໃນເດັກນ້ອຍ. ໃນປະມານ 75% ຂອງກໍລະນີ, ບາດແຜເຫຼົ່ານີ້ສະແດງໃຫ້ເຫັນໃນປີທຳອິດຂອງຊີວິດ, ແລະຫຼາຍກວ່າ 15‑20% ຂອງຜູ່ເຈັບມີພວກມັນຕັ້ງແຕ່ເກີດ. ໃນຜູ່ໃຫຍ່, JXG ມັກເກີດຂຶ້ນໃນອາຍຸ 20‑30 ປີ, ແລະຜູ່ໃຫຍ່ສ່ວນໃຫຍ່ມີບາດແຜດຽວ. ທາງການຄລິນິກ, ມັນປະກົດເປັນຕຸ່ມຫຼື ກ້ອນສີເຫຼືອງ‑ສີສົ້ມ‑ສີນ້ຳຕານ, ສ່ວນຫຼາຍຢູ່ໜ້າ, ຄໍ ແລະ ຮ່າງກາຍສ່ວນເທິງ. ບາດແຜໃນປາກອາດເປັນກ້ອນສີເຫຼືອງຢູ່ຂ້າງຂອງລີ້ນ ຫຼື ບ່ອນອື່ນໃນປາກ, ອາດເຮັດໃຫ້ເກີດບາດແຜ ແລະ ເລືອດອອກ. ບາດແຜຜິວບໍ່ເຮັດໃຫ້ເກີດອາການ ແລະມັກຈະຫາຍໄປເອງໃນຫຼາຍປີ. ນອກຈາກຜິວຫນັງ, ການມີສ່ວນຮ່ວມຂອງຕາແມ່ນບັນຫາທົ່ວໄປທີ່ສຸດ. Ocular JXG ສ່ວນໃຫ້ຜົນກະທົບຕໍ່ຕາດຽວ ແລະເກີດຂຶ້ນໃນຜູ່ທີ່ນ້ອຍກວ່າ 0.5% ຂອງຜູ່ເຈັບ, ແຕ່ປະມານ 40% ຂອງຜູ່ທີ່ມີການມີສ່ວນຮ່ວມຂອງຕາ ຍັງມີບາດແຜຜິວຫນັງຫຼາຍຄັ້ງເມື່ອກວດພົບ.
Juvenile xanthogranuloma (JXG) is a relatively common entity and is the most common form of non-Langerhans cell histiocytic disorder of childhood., It is estimated that in 75% of cases, lesions appear during the first year of life, with >15-20% of patients having lesions at birth. JXG is rare in adults, with a peak incidence in the late twenties to thirties. The majority of adult patients have solitary lesions. Typically, the clinical presentation consists of solitary or multiple yellow-orange-brown firm papules or nodules. The most common locations are the face, neck, and upper torso. Oral lesions are rare and often occur as a yellow nodule on the lateral aspects of the tongue. Oral lesions can also arise on the gingival, buccal mucosa, and midline hard palate and may ulcerate and bleed. Cutaneous lesions are usually asymptomatic, and most lesions spontaneously involute over the course of several years. Although occurring rarely, ocular involvement is the most common extracutaneous site involved, followed by the lungs. Ocular JXG is nearly always unilateral and develops in less than 0.5% of patients. Approximately 40% of patients with ocular JXG, however, have multiple cutaneous lesions at the time of diagnosis.
Juvenile xanthogranuloma (JXG) is a relatively common entity and is the most common form of non-Langerhans cell histiocytic disorder of childhood., It is estimated that in 75% of cases, lesions appear during the first year of life, with >15-20% of patients having lesions at birth. JXG is rare in adults, with a peak incidence in the late twenties to thirties. The majority of adult patients have solitary lesions. Typically, the clinical presentation consists of solitary or multiple yellow-orange-brown firm papules or nodules. The most common locations are the face, neck, and upper torso. Oral lesions are rare and often occur as a yellow nodule on the lateral aspects of the tongue. Oral lesions can also arise on the gingival, buccal mucosa, and midline hard palate and may ulcerate and bleed. Cutaneous lesions are usually asymptomatic, and most lesions spontaneously involute over the course of several years. Although occurring rarely, ocular involvement is the most common extracutaneous site involved, followed by the lungs. Ocular JXG is nearly always unilateral and develops in less than 0.5% of patients. Approximately 40% of patients with ocular JXG, however, have multiple cutaneous lesions at the time of diagnosis.
Juvenile xanthogranuloma (JXG) ເປັນພະຍາດທີ່ບໍ່ທຳມະດາ, ເປັນພະຍາດທີ່ເປັນສ່ວນໜຶ່ງຂອງປະເພດໃຫຍ່ຂອງ non‑Langerhans cell histiocytoses. ໂດຍປົກກະຕິແລ້ວພວກມັນຈະປາກົດເປັນກ້ອນໜຶ່ງ ຫຼືຫຼາຍກ້ອນສີແດງ ຫຼືສີເຫຼືອງ, ມັກຈະພົບເຫັນຢູ່ຫົວ ຫຼືຄໍ. JXG ສ່ວນໃຫຍ່ພັດທະນາໃນເວລາເກີດຫຼືໃນປີທໍາອິດຂອງຊີວິດ. ໃນຂະນະທີ່ບໍ່ປົກກະຕິ, ບາງຄັ້ງພວກມັນສາມາດສົ່ງຜົນກະທົບຕໍ່ພື້ນທີ່ນອກເຫນືອຜິວຫນັງ, ດ້ວຍການມີການສ່ວນຮ່ວມຂອງຕາເປັນສິ່ງທີ່ຕ້ອງສັງເກດເບິ່ງຕາມວັນນະຄະດີທີ່ມີຢູ່. ໂດຍທົ່ວໄປແລ້ວ, JXG ໃນຜິວຫນັງຈະຫາຍໄປດ້ວຍຕົວມັນເອງ ແລະ ດ້ວຍປົກກະຕິ ບໍ່ຈໍາເປັນຕ້ອງການການຮັບ.
Juvenile xanthogranulomas (JXGs) are uncommon, benign diseases that are part of a larger category of non-Langerhans cell histiocytoses. They typically show up as one or more red or yellowish lumps, often found on the head or neck. Most JXGs develop either at birth or within the first year of life. While it's unusual, sometimes they can affect areas beyond the skin, with eye involvement being something to watch for according to existing literature. Generally, JXGs on the skin go away on their own and typically don't need treatment.
Juvenile xanthogranulomas (JXGs) are uncommon, benign diseases that are part of a larger category of non-Langerhans cell histiocytoses. They typically show up as one or more red or yellowish lumps, often found on the head or neck. Most JXGs develop either at birth or within the first year of life. While it's unusual, sometimes they can affect areas beyond the skin, with eye involvement being something to watch for according to existing literature. Generally, JXGs on the skin go away on their own and typically don't need treatment.
ການກ່ຽວຂ້ອງຕາ (ocular involvement) ອອກໃນເຖິງ 10% ຂອງປະຊາຊົນທີ່ມີ JXG ແລະອາດຈະສົ່ງຜົນກະທົບຕໍ່ການເບິ່ງເຫັນຂອງເຂົາເຈົາ. ເຖິງວ່າບາດແຜຕາມຜິວນັງຈະຫາຍໄປເອງຕາມລຳດັບ, ແຕ່ບາດແຜທາງຕາບໍ່ຄ່ອຍຈະດີຂຶ້ນເອງ ແລະຕ້ອງການການປິ່ນປົວ.