1.Recurred Adenoid Cystic Carcinoma of Lacrimal Gland with Aggressive Local Invasion to the Maxillary Bone Marrow without Increased Uptake in PET-CT.
Moonjung CHOI ; Ja Seung KOO ; Jin Sook YOON
Korean Journal of Ophthalmology 2015;29(1):68-70
No abstract available.
Bone Marrow/*pathology/radiography/radionuclide imaging
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Carcinoma, Adenoid Cystic/*diagnosis
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Eye Neoplasms/*diagnosis
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Female
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Humans
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Lacrimal Apparatus/*pathology/radiography/radionuclide imaging
;
Lacrimal Apparatus Diseases/*diagnosis
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Maxilla
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Middle Aged
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Neoplasm Invasiveness
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Neoplasm Recurrence, Local
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*Positron-Emission Tomography
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*Tomography, X-Ray Computed
3.Cyst of accessory lacrimal gland.
Korean Journal of Ophthalmology 1995;9(2):117-121
When a patient is presented with a subconjunctival cyst, it is not only hard to reveal its true nature clinically but also easy to rupture during excision. We experienced cases with cysts of the accessory lacrimal gland in two patients with subconjunctival cysts. They had lid swelling at initial presentation and underwent surgical excision of subconjunctival cysts located in superior portion of the upper tarsal plate. The lining of these cysts composed of ductal epithelia. Biochemical analyses for serum and cystic fluid were performed in one case, in which was found high Ig A titer in the cystic fluid. These cysts seemed to originate from the duct of Wolfring's accessory lacrimal gland, considering their anatomic locations and pathologic findings. Complete removal of the cyst is important, because recurrences have been reported in cases of incomplete removal or simple aspiration.
Adult
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Conjunctival Diseases/pathology/surgery
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Cysts/*pathology/surgery
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Female
;
Humans
;
Lacrimal Apparatus Diseases/*pathology/surgery
;
Orbit/radiography
;
Tomography, X-Ray Computed
4.The Radiological Spectrum of Orbital Pathologies that Involve the Lacrimal Gland and the Lacrimal Fossa.
Won Sang JUNG ; Kook Jin AHN ; Mi Ra PARK ; Ji Young KIM ; Jae Jeong CHOI ; Bum Soo KIM ; Seong Tai HAHN
Korean Journal of Radiology 2007;8(4):336-342
CT and MRI are utilized to differentiate between different types of masses and to determine the extent of lesions involving the lacrimal gland and the fossa. Although many diseases that affect the lacrimal gland and fossa are specifically diagnosed by imaging, it is frequently very difficult to differentiate each specific disease on the basis of image characteristics alone due to intrinsic similarities. In lacrimal gland epithelial tumors, benign pleomorphic adenomas are seen most commonly with a well defined benign appearance, and a malignant adenoid cystic carcinoma is seen with a typical invasive malignant appearance. However, a malignant myoepithelial carcinoma is seen with a benign looking appearance. Lymphomatous lesions of the lacrimal gland include a broad spectrum ranging from reactive hyperplasia to malignant lymphoma. These lesions can be very difficult to differentiate both radiologically and pathologically. Generally, lymphomas tend to occur in older patients. The developmental cystic lesions found in the lacrimal fossa such as dermoid and epidermoid cysts can be diagnosed when the cyst involves the superior temporal quadrant of the orbit and manifests as a non-enhancing cystic mass and, in case of a lipoma, it is diagnosed as a total fatty mass. However, masses of granulocytic sarcoma and xanthogranuloma, as well as vascular masses, such as a hemangiopericytoma, are difficult to diagnose correctly on the basis of preoperative imaging findings alone. A careful clinical evaluation and moreover, a pathologic verification, are needed. In this pictorial review, the various imaging spectrums of pathologic masses involving the lacrimal gland and fossa are presented, along with appropriate anatomy and pathology reviews.
Carcinoma, Squamous Cell/radiography
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Conjunctival Neoplasms/radiography
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Cysts/radiography
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Eye Neoplasms/*radiography
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Hemangiopericytoma/radiography
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Humans
;
Lacrimal Apparatus/*pathology
;
Lacrimal Apparatus Diseases/radiography
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Lipoma/radiography
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Lymphoma/radiography
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Neoplasms, Glandular and Epithelial/radiography
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Neurofibroma/radiography
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Sarcoma, Myeloid/radiography
5.Case Reports of Lacrimal Sac Tumors Discovered in Patients with Persistent Epiphora Following Dacryocystorhinostomy.
Ka Hyun LEE ; Sun Hyup HAN ; Jin Sook YOON
Korean Journal of Ophthalmology 2015;29(1):66-67
No abstract available.
Aged
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Biopsy
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Carcinoma, Squamous Cell/diagnosis/*etiology
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Dacryocystorhinostomy/*adverse effects
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Eye Neoplasms/diagnosis/*etiology
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Female
;
Humans
;
Lacrimal Apparatus/pathology/*surgery
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Lacrimal Apparatus Diseases/diagnosis/*etiology
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*Postoperative Complications
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Tomography, X-Ray Computed
6.Clinical analysis of nasal sinus mucocele with eye symptoms as main manifestation: 3 cases report.
GU QINGJIA ; LI JINGXIAN ; FAN JIANGANG
Journal of Clinical Otorhinolaryngology Head and Neck Surgery 2015;29(7):666-667
Endoscopic sinus surgery is effective to nasal sinus mucocele with eye symptoms as main manifestation. It is very importment to raise the awareness of the disease and to prompt imaging examination. Three cases were reviewed. One mucocele was found in the frontal sinus ethmoid sinus,1 in the fronto-ethmoid sinus and 1 in the spheno-ethmoid sinus. All cases were preoperatively diagnosed by CT, MRI or intranasal endoscopy. Nasal sinus mucocele with eye symptoms as main manifestation should be early diagnosed. Endoscopic sinus surgery is a safe and effective method for the treatment of nasal sinus mucocele,and could be the primary choice for it. All cases were treated by nasal endoscopic sinus surgery. The majority of symptoms, such as exophthalmos, epiphora and diplopia, disappeared in all patients. However, vision recovery was observed only in some patients.
Diplopia
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complications
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Endoscopy
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Ethmoid Sinus
;
pathology
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Exophthalmos
;
complications
;
Frontal Sinus
;
pathology
;
Humans
;
Lacrimal Apparatus Diseases
;
complications
;
Magnetic Resonance Imaging
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Mucocele
;
complications
;
diagnosis
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Paranasal Sinus Diseases
;
complications
;
diagnosis
7.Hemangiopericytoma of the lacrimal sac.
Key Hwan LIM ; Yoon Duck KIM ; Yong Il KIM
Korean Journal of Ophthalmology 1991;5(2):88-91
Hemangiopericytomas are soft tissue tumors composed of pericapillary pericytes. These tumors are rare in the lacrimal sac. To the author's knowledge, only four previous cases of these tumors occurring in the lacrimal sac have been reported. A primary hemangiopericytoma of the lacrimal sac in a 34-year-old female is reported. Total excision with the surrounding tissue appears to be the treatment of choice for this tumor.
Adult
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Eye Neoplasms/*pathology/radiography/surgery
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Female
;
Hemangiopericytoma/*pathology/radiography/surgery
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Humans
;
Lacrimal Apparatus Diseases/*pathology/radiography/surgery
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Tomography, X-Ray Computed
8.Management of Dermoid Tumor in the Medial Canthal Area.
Nam Ju KIM ; Ho Kyung CHOUNG ; Sang In KHWARG
Korean Journal of Ophthalmology 2009;23(3):204-206
Dermoid tumors in the medial canthal area are rare, but when present they commonly adhere to the lacrimal canaliculi. Three patients presented with a mass in the medial canthal area. The authors performed excisional biopsies, and the masses were diagnosed as dermoid tumors. In two patients, canalicular lacerations were found after mass excision, which suggested that the masses had been firmly adherent to the lacrimal canaliculi. The lacerated canaliculi were repaired after bicanalicular silicone intubation. In the remaining patient, lacrimal silicone intubation was performed at the beginning of surgery, and the mass was successfully dissected from the canaliculi, leaving them intact. Excision of dermoid tumors in the medial canthal area requires careful dissection to avoid canalicular laceration. Bicanalicular silicone intubation at the beginning of surgery is helpful for the identification of the canaliculi and for the prevention of canalicular laceration during dermoid tumor excision.
Adolescent
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Adult
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Dermoid Cyst/pathology/*surgery
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Female
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Humans
;
Intubation
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Lacrimal Apparatus Diseases/pathology/*surgery
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Male
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Middle Aged
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Orbital Neoplasms/pathology/*surgery
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Postoperative Care
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Preoperative Care
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Silicones
9.A Case of Giant Fronto-Ethmoidal Osteoma using rib and Calvarial Bone Graft.
Nak Jin CHOI ; Jun Pyo KIM ; Sung Hee HONG ; Hee In KANG
Journal of the Korean Cleft Palate-Craniofacial Association 2003;4(1):62-65
Osteoma is a slowly growing benign tumor which mainly grows on the mandible and in the paranasal sinuses of the craniofacial region. Embryological, inflammatory, and traumatic theories make up the etiological basis of osteoma, but is still unclear and yet to be studied. We can classify osteoma by morphology and pathology into eburnated, cancellous, and mixed type, of which eburnated type is relatively common. Most osteomas accompany no symptoms, so they are often discovered accidentally by a radiological examination. They never develop into a malignant form, so that periodic observation is sufficient enough for management, but when they grow and invade intraorbitally or intracranially and then compress clinically important structures, need a surgical management, because of possibility of diplopia, exophthalmos, epiphora, blindness due to optic atrophy, mucocele, brain abscess, meningitis. A 52-year-old man complaining of right eye pain, diplopia, and exophthalmos was diagnosed a 4.5x3.0x 2.0cm sized fronto-ethmoidal osteoma by means of a three dimensional computed tomography. We experienced a osteoma removal through bicoronal incision, and orbital reconstruction with both rib and calvarial bone graft, and received satisfying results after 1 year follow-up, thereby report this case with a short review of references.
Blindness
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Brain Abscess
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Diplopia
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Exophthalmos
;
Eye Pain
;
Follow-Up Studies
;
Humans
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Lacrimal Apparatus Diseases
;
Mandible
;
Meningitis
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Middle Aged
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Mucocele
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Optic Atrophy
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Orbit
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Osteoma*
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Paranasal Sinuses
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Pathology
;
Ribs*
;
Transplants*
10.Clinical research on benign lymphoepithelial lesions of lacrimal gland in 20 Chinese patients.
Jian-Min MA ; Jing LI ; Xin GE ; Ming LI ; Jin-Ru LI ; Xiao-Na WANG
Chinese Medical Journal 2015;128(4):493-498
BACKGROUNDBenign lymphoepithelial lesion (BLEL) is characterized by symmetric bilateral swelling of the lacrimal and salivary glands and considered a subtype of immunoglobulin G4 (IgG4)-related sclerosing disease, the etiology and pathogenesis of which has not been determined. The purpose of the present study was to analyze the clinical features of BLEL in the lacrimal gland and the relationship between the serum level of IgG4 and BLEL.
METHODSTwenty consecutive patients with BLEL diagnosed in Department of Ophthalmology at Beijing Tongren Hospital, Capital Medical University between January 2012 and December 2013 were observed. The clinical features, imaging findings, laboratory tests, treatments and follow-up status of these 20 consecutive patients were analyzed.
RESULTSIn all 20 patients, the ratio of male to female was 1:4, the ages ranged from 28 to 57 years, the ratio of unilateral to bilateral eyes involvement was 1:4, and painless uncongested symmetrical swelling of the upper eyelid was the main clinical manifestation. Orbital magnetic resonance imaging (MRI) showed that all patients involved lacrimal gland, which were obviously enlarged with equal signals in T1W images and T2W images and obvious enhancement on contrast MRI. Extraocular muscles were involved in 5 patients, salivary gland in 8 patients, and frontal nerve in 3 patients. Serum IgG4 concentration was elevated in 18 patients. The treatment strategy mainly included surgery and steroid administration. Three patients were lost to follow-up, 17 patients reached complete response, and no recurrence was observed.
CONCLUSIONSEyelid swelling is the typical symptom of BLEL. Most of the patients involved bilateral lacrimal glands. High serum IgG4 level and abundant IgG4-positive plasma cell infiltration are the important features, which can be found in most of BLEL patients. Surgery combined with glucocorticoids is an efficient treatment strategy.
Adult ; Female ; Glucocorticoids ; therapeutic use ; Humans ; Immunoglobulin G ; blood ; Lacrimal Apparatus ; pathology ; Lymphatic Diseases ; blood ; diagnosis ; drug therapy ; surgery ; Male ; Middle Aged