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mucocele/ödéma

A hivatkozás a vágólapra kerül
CikkekKlinikai vizsgálatokSzabadalmak
Oldal 1 tól től 28 eredmények

Mucocele formation 20 years after an appendiceal uterine transplantation for infertility mistaken for hydrops tubae profluens.

Csak regisztrált felhasználók fordíthatnak cikkeket
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A 56 year old woman was admitted to our hospital with a 9-year history of recurrent, lower abdominal pain and mucoid vaginal discharge 20 years after an appendiceal uterine transplantation. The removal of the uterus and the attached appendix resulted in the disappearance of the symptoms. A mechanism

[Myopic astigmatism, unilateral exophthalmos and retinal edema caused by mucocele of the ethmoid sinus].

Csak regisztrált felhasználók fordíthatnak cikkeket
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[Unilateral Papillary Edema Due to Sinus Mucocele].

Csak regisztrált felhasználók fordíthatnak cikkeket
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[Sphenoid sinus mucocele with recurrent visual disturbance].

Csak regisztrált felhasználók fordíthatnak cikkeket
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We presented a case with sphenoid sinus mucocele associated with recurrent visual disturbance on the same side. A 22-year-old female showed two episodes of visual disturbance on the left eye for three months. She was diagnosed as acute retrobulbar optic neuritis and was treated with cortico-steroid.

Facial mucocele and brain complications: diagnostic priorities.

Csak regisztrált felhasználók fordíthatnak cikkeket
Belépés Regisztrálás
We present the case of a male with a history of nasal polyposis underwent bilateral nasosinusal endoscopic surgery. He went to the emergency department because of having behavioral changes and left frontal headache. An emergency CT showed nasal-sinus polyposis and several nodular lesions with a

Excision of Mucocele Using Diode Laser in Lower Lip.

Csak regisztrált felhasználók fordíthatnak cikkeket
Belépés Regisztrálás
Mucoceles are nonneoplastic cystic lesions of major and minor salivary glands which result from the accumulation of mucus. These lesions are most commonly seen in children. Though usually these lesions can be treated by local surgical excision, in our case, to avoid intraoperative surgical

Three cases of isolated mucoceles and one case of an Aspergillus infection in the sphenoid sinus with orbital signs and symptoms.

Csak regisztrált felhasználók fordíthatnak cikkeket
Belépés Regisztrálás
Four patients with an isolated sphenoid lesion: three with a mucocele and one with an Aspergillus infection of the sphenoid sinus in whom the orbital impairment had a rhinogenic cause, are described. They all presented with one or more of the following features: visual loss, motility disturbances,

[Frontal sinusitis, mucocele and subperiosteal superolateral orbit abscess].

Csak regisztrált felhasználók fordíthatnak cikkeket
Belépés Regisztrálás
BACKGROUND Periorbital infection following pansinusitis is a rare complication which can lead to irreversible orbital and intracranial consequences. Chandler classified them in 1970. METHODS An eight-year-old child presented with a subperiosteal superolateral abscess. The initial flu-like syndrome

Intestinal strangulation caused by a mucocele of the appendix: report of a case.

Csak regisztrált felhasználók fordíthatnak cikkeket
Belépés Regisztrálás
Intestinal strangulation caused by a mucocele of the appendix is extremely rare and difficult to diagnose. It is not usually suspected pre-operatively. This report presents a case of intestinal strangulation due to a mucous containing cystic lesion that was wrapped around the base of a loop of the

Orbital and Eyelid Inflammation With "Muciphages" and Extravasated Mucin From an Ethmoido-orbital Mucocele.

Csak regisztrált felhasználók fordíthatnak cikkeket
Belépés Regisztrálás
A 22-year-old woman presented with an acute compressive optic neuropathy due to a ruptured ethmoido-orbital mucocele. She underwent urgent orbital decompression and drainage of the mucocele via an endoscopic approach. Postoperatively, her course was complicated by an orbital compartment syndrome

Mucocele: a human model for lymphangiogenesis.

Csak regisztrált felhasználók fordíthatnak cikkeket
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The mechanism of lymphangiogenesis is poorly understood, and controversy exists whether it is part of the inflammatory response to tissue injury. Utilizing markers specific to lymphatics, we aimed to study if lymphangiogenesis plays a role in the tissue response of mucoceles. Twenty-three

[Pediatric acute dacryocystitis due to frontoethmoidal mucocele].

Csak regisztrált felhasználók fordíthatnak cikkeket
Belépés Regisztrálás
Pediatric acute dacryocystitis typically develops due to persistence of Hasner's membrane. Pediatric paranasal mucoceles are rare entities. In contrast, chronic dacryocystitis in cases of congenital dacryostenosis is one of the most frequent pediatric ophthalmologic

[A case of appendiceal mucocele associated with cancer of the colon].

Csak regisztrált felhasználók fordíthatnak cikkeket
Belépés Regisztrálás
Mucocele of the appendix is a rare lesion (only 0;2-0.3% of all appendicectomies). It is characterized by distension of the lumen within mucus. Mucoceles are often asymptomatic and are discovered as an incidental finding either at surgery or during barium edema. There have been reports of other

[Two cases of intussusception of appendiceal mucocele: diagnostic value of preoperative ultrasonography].

Csak regisztrált felhasználók fordíthatnak cikkeket
Belépés Regisztrálás
Mucocele of the appendix was first described and named "Hydrops processus vermiformis" by Rokitansky in 1866. Intussusception of a appendiceal mucocele is very rare and we have been able to find only 14 previously reported cases. We present two cases with preoperative ultrasonography which is

Laryngeal Myxoglobulosis: A Rare Histologic Variant of Mucocele. The First Reported Case.

Csak regisztrált felhasználók fordíthatnak cikkeket
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Myxoglobulosis is a rare histologic variant of mucocele that is characterized by transformation of mucin into eosinophilic globules. The globules frequently demonstrate a lamellar pattern and are surrounded by an inflammatory cell infiltrate. Myxoglobulosis has not yet been described in laryngeal
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