Lymphangioma
Lymphangioma kukanganisa kwe lymphatic system inoratidzwa nemaronda ari matete-walled cysts. Izvi zvinokanganisa zvinogona kuitika chero nguva ipi zvayo uye zvinogona kusanganisira chero chikamu chemuviri, asi 90% inoitika muvana vari pasi pemakore maviri uye inosanganisira musoro nemutsipa.Lymphangiomas inowanzoongororwa vasati vaberekwa vachishandisa fetal ultrasonography. Inowanikwa lymphangiomas inogona kuguma nekushungurudzika, kuzvimba, kana kuvharwa kwe lymphatic. Sezvo vasina mukana wekuve nehutsinye, lymphangiomas inowanzorapwa nekuda kwezvikonzero zvekushongedza chete.
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References
Lymphangioma inozivikanwawo se lymphatic malformation (LM) . Chirwere chevascular chiripo kubva pakuzvarwa. Inoratidzwa nekusakura kusiri kujairika kwetishu ye lymphatic pamberi uye mushure mekuzvarwa. Lymphangioma inokanganisa munhu mumwe chete muna 2000 kusvika ku4000 vanhu, pasina mutsauko wakakura pakati pevarume kana madzinza. Zviitiko zvizhinji (80-90%) zvinoonekwa vasati vasvika makore maviri. Zviratidzo zvinosiyana zvakasiyana-siyana, kubva pakuzvimba kwenzvimbo kusvika kune zvakakura zvisina kujairika mumigwagwa ye lymphatic, dzimwe nguva zvichitungamira mukuzvimba kwakanyanya kunozivikanwa seelephantiasis. Semuenzaniso, lymphangioma mumutsipa uye chiso zvinogona kukonzera kuzvimba kwechiso, uye mumatambudziko akaoma, kukanganisa. Kana ichikanganisa rurimi, inogona kutungamirira kukukura kweshaya uye mazino asina kurongeka. Mumuromo nemumutsipa, zvinogona kukonzera matambudziko ekufema uye njodzi dzinotyisa dzehupenyu. Mumaziso, zvinogona kukonzera kurasikirwa kwekuona, kufamba kwemaziso kushoma, ziso rakarembera, uye maziso akatsvuka. Kubatanidzwa kwemakumbo kunogona kukonzera kuzvimba uye kukura kusiri kwemaitiro ematishu nemapfupa. Bundu iri rinowanzokura zvishoma nezvishoma, asi utachiona, kuchinja kwehomoni, kana kukuvara kunogona kukonzera kukura nekukurumidza, zvichiunza njodzi dzinotyisa dzinoda kurapwa nekukurumidza.
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.
Muchidzidzo chekudzoka shure, takaongorora vana makumi maviri nevana vaiva ne lymphangioma uye vakarapwa nemajekiseni ebleomycin kubva muna Ndira 1999 kusvika Zvita 2004. Maronda mazhinji (63%) akapera zvachose, 21% akawana mhinduro yakanaka, uye 16% haana kupindura zvakanaka. Varwere vaviri vakaita bundu racho rikazodzoka pave paya, uye vamwe vaviri vakaita matumbu kwavakabaiwa majekiseni. Sezvineiwo, hatina kuona mamwe matambudziko makuru kana mhedzisiro.
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.
Mhando huru dze lymphangioma ndedzinotevera - lymphangioma circumscriptum, cavernous lymphangioma, cystic hygroma, lymphangioendothelioma. Izvi zvinoumba zvikamu makumi maviri nenhanhatu kubva muzana zvezvironda zvemudumbu muvana asi zvisingawanikwe muvakuru. Lymphangioma circumscriptum , imhando inowanzoitika, inoratidza ma lymphatic ducts akabudikira mukati meganda, achigadzira ma vesicles akajeka akazadzwa nemvura akafanana netatya kuzvara, pamwe nekuzvimba kwenyama. Inowanzoonekwa munzvimbo dzine hupfumi hwe lymphatic network semakumbo, trunk, uye armpits. Mumwe mukadzi ane makore 71 akauya kukiriniki yedu achiramba achizvimba gumbo, mapundu epingi panhengo yake yokubereka nayo, kuvava, uye kubuda mvura yelymph. Takavhiya mabumps ese nemaitiro anonzi bilateral major labiectomy, tichimira paColles' fascia level, tichichengetedza clitoris nefourchette.
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.
