1.Skin malignancy initially misdiagnosed as a benignepidermal cyst
Chan Min CHUNG ; Sung Jae WEE ; Hyoseob LIM ; Sang Hun CHO ; Jong Wook LEE
Archives of Craniofacial Surgery 2020;21(2):123-126
Skin cancer, which often occurs as a result of skin exposure to ultraviolet light radiation, usuallypresents with characteristic abnormal features, such as ulcerative lesions, irregular morphology,bleeding, and excessive growth. Therefore, skin cancer rarely resembles a benign tumor on visualinspection. Nonetheless, squamous cell carcinoma and basal cell carcinoma with nodular or polypoidfeatures can have a similar appearance to that of benign tumors, meaning that they aresometimes misdiagnosed as benign. As benign and malignant tumors have some overlappingfeatures, clinicians sometimes use additional imaging techniques such as ultrasonography to improvethe accuracy of the diagnosis because even a malignant tumor that externally resembles abenign tumor generally has internal morphological features characteristic of malignancy, such asinvasion and irregular borders. However, these imaging tools also have limitations, and punch orexcisional biopsy can be needed if malignancy cannot be completely ruled out. Herein, we reporta case of skin malignancy initially misdiagnosed as a benign epidermal cyst based on external visualinspection and ultrasonography.
2.Early management of parotid gland injury with oral nortriptyline and closed drain
Chan Min CHUNG ; Sung Jae WEE ; Hyoseob LIM ; Sang Hun CHO ; Jong Wook LEE
Archives of Craniofacial Surgery 2020;21(4):253-256
Parotid gland plays the most critical role in saliva secretion in the oral cavity. Parotid gland injuries due to facial trauma can cause various complications such as formation of a fistula or sialocele. Thus, such saliva-related complications can interfere with wound healing and increase the risk of infection. Several previous studies have discussed the treatment of fistula or sialocele. Nonetheless, prevention of such complications is of utmost importance. We present a case of parotid gland injury due to trauma to the cheeks that was surgically treated, with early postoperative management involving oral administration of nortriptyline and closed drainage, without complications.
3.Urinary transglutaminase 2 as a potent biomarker to predict interstitial fibrosis and tubular atrophy of kidney allograft during early posttransplant period in deceased donor kidney transplantation
Jee Yeon KIM ; Yu Mee WEE ; Monica Young CHOI ; Hey Rim JUNG ; Ji Yoon CHOI ; Hyun Wook KWON ; Joo Hee JUNG ; Yong Mee CHO ; Heounjeong GO ; Minkyu HAN ; Young Hoon KIM ; Duck Jong HAN ; Sung SHIN
Annals of Surgical Treatment and Research 2019;97(1):27-35
PURPOSE: Transglutaminase type 2 (TG2) is an extracellular matrix crosslinking enzyme with a pivotal role in kidney fibrosis. We tested whether quantification of urinary TG2 may represent a noninvasive method to estimate the severity of kidney allograft fibrosis. METHODS: We prospectively collected urine specimens from 18 deceased donor kidney transplant recipients at 1-day, 7-day, 1-month, 3-month, and 6-month posttransplant. In addition, kidney allograft tissue specimens at 0-day and 6-month posttransplant were sampled to analyze the correlation of urinary TG2 and kidney allograft fibrosis. RESULTS: Thirteen recipients had increased interstitial fibrosis and tubular atrophy (IFTA) scores at the 6-month protocol biopsy (IFTA group). The mean level of urinary TG2 in the IFTA group was higher compared to that of 5 other recipients without IFTA (no IFTA group). Conversely, the mean level of urinary syndecan-4 in the IFTA group was lower than levels in patients without IFTA. In the IFTA group, double immunofluorescent staining revealed that TG2 intensity was significantly upregulated and colocalizations of TG2/heparin sulfate proteoglycan and nuclear syndecan-4 were prominent, usually around tubular structures. CONCLUSION: Urinary TG2 in early posttransplant periods is a potent biomarker for kidney allograft inflammation or fibrosis.
Allografts
;
Atrophy
;
Biomarkers
;
Biopsy
;
Extracellular Matrix
;
Fibrosis
;
Humans
;
Inflammation
;
Kidney Transplantation
;
Kidney
;
Methods
;
Prospective Studies
;
Proteoglycans
;
Syndecan-4
;
Tissue Donors
;
Transplant Recipients
4.Angiogenin for the Diagnosis and Grading of Dry Eye Syndrome.
Won Soo KIM ; Sung Wook WEE ; Seung Hoon LEE ; Jae Chan KIM
Korean Journal of Ophthalmology 2016;30(3):163-171
PURPOSE: To investigate the properties of angiogenin (ANG) as a potential tool for the diagnosis and grading of dry eye syndrome (DES) by analyzing tear protein profiles. METHODS: Tear samples were collected with capillary tubes from 52 DES patients and 29 normal individuals as controls. Tear protein profiles were analyzed with an immunodot blot assay as a screening test. To confirm that the tear ANG levels were in inverse proportion to the disease severity grade, the ANG and lactoferrin (LF) tear contents of normal controls and DES patients were compared in an enzyme-linked immunosorbent assay. RESULTS: In the immunodot blot assay, the ANG area was lower in patients with grades 3 and 4 DES than in normal controls. The areas of basic fibroblast growth factor, transforming growth factor β2, and interleukin 10 were significantly greater than those of normal controls only in grade 4 DES patients, but these proteins were not linearly correlated with dry eye severity. Upon enzyme-linked immunosorbent assay analysis, the mean concentrations of ANG and LF decreased significantly as dry eye severity increased, except between grades 1 and 2. In addition, the ratios of ANG and LF to total tear proteins were correlated significantly with DES severity. CONCLUSIONS: ANG level was significantly lower in DES patients than in normal controls, and was significantly correlated with the worsening severity of DES, except between grades 1 and 2, as was LF. Therefore, ANG may be a useful measure of DES severity through proteomic analysis.
Adult
;
Aged
;
Angiogenesis Inducing Agents/pharmacology
;
Dry Eye Syndromes/*diagnosis/metabolism
;
Enzyme-Linked Immunosorbent Assay
;
Female
;
Follow-Up Studies
;
Humans
;
Immunoblotting
;
Male
;
Middle Aged
;
Proteomics/methods
;
Ribonuclease, Pancreatic/*pharmacology
;
Severity of Illness Index
;
Tears/chemistry
;
Young Adult
5.Deep Anterior Lamellar Keratoplasty Using Irradiated Acellular Cornea with Amniotic Membrane Transplantation for Intractable Ocular Surface Diseases.
Sung Wook WEE ; Sang Uk CHOI ; Jae Chan KIM
Korean Journal of Ophthalmology 2015;29(2):79-85
PURPOSE: To report the clinical outcomes of deep anterior lamellar keratoplasty (DALK) when sterile gamma-irradiated acellular corneal tissues (VisionGraft) are used in combination with amniotic membrane transplantation (AMT) for intractable ocular surface diseases. METHODS: The medical records of fifteen patients who had DALK with AMT were retrospectively reviewed. Indications for surgery included ocular burn, bacterial keratitis, herpes simplex virus keratitis, corneal opacity with Stevens-Johnson syndrome, Mooren's ulcer, idiopathic myxoid degeneration of corneal stroma, and recurrent band keratopathy. DALK was performed using partial-thickness acellular corneal tissue and a temporary amniotic membrane patch was added at the end of the operation. RESULTS: All cases that underwent DALK with AMT became epithelialized within 2 postoperative weeks. Twelve patients showed favorable outcomes without graft rejection, corneal opacification, or neovascularization. The other three grafts developed corneal opacification and neovascularization, and required additional penetrating keratoplasty (PK). Unlike the results of previous PKs, there were no graft rejections and the graft clarity was well-maintained in these three cases for at least 8 months after PK. CONCLUSIONS: DALK using sterile acellular corneal tissues in combination with AMT may be a good therapeutic strategy for treating intractable ocular surface diseases because of lowered immune rejection, fibroblast activation, and facilitation of epithelialization. Furthermore, DALK can help stabilize the ocular surface, prolong graft survival, and may allow better outcomes when combined with subsequent PK.
Adult
;
Aged
;
Amnion/*transplantation
;
Corneal Diseases/pathology/*surgery
;
Corneal Stroma/radiation effects/*transplantation
;
Female
;
Graft Survival
;
Humans
;
Keratoplasty, Penetrating/*methods
;
Male
;
Middle Aged
;
Retrospective Studies
;
Visual Acuity
;
Young Adult
6.Treatment of an 8-mm Myxoma Using Acellular Corneal Tissue.
Kyung Sup LIM ; Sung Wook WEE ; Jae Chan KIM
Korean Journal of Ophthalmology 2014;28(1):86-90
A myxoma is a benign tumor found in the heart and in various soft tissues; however, a corneal myxoma is rare. A mucinous mass of unknown etiology was observed on the left cornea of a 32-year-old male patient. We performed deep anterior lamellar keratoplasty using acellular corneal tissue and concurrent amniotic membrane transplantation. Hematoxylin and eosin staining revealed vacuolation of the parenchyma and myxoid change in the corneal tissue that occurred in the anterior half of the corneal parenchyma. We identified a myxoid stroma by Alcian blue staining and observed collagen fibers with denatured stroma by Masson trichrome staining. The patient's visual acuity improved from light perception to 20 / 200, and the intraocular pressure remained within the normal range for one year after surgery. The transplanted cornea survived successfully with well-maintained transparency, and recurrence was not observed one year after surgery.
Adult
;
*Cornea
;
Corneal Stroma/cytology/*transplantation
;
Corneal Transplantation/*methods
;
Eye Neoplasms/diagnosis/*surgery
;
Humans
;
Male
;
Myxoma/diagnosis/*surgery
7.Treatment of an 8-mm Myxoma Using Acellular Corneal Tissue.
Kyung Sup LIM ; Sung Wook WEE ; Jae Chan KIM
Korean Journal of Ophthalmology 2014;28(1):86-90
A myxoma is a benign tumor found in the heart and in various soft tissues; however, a corneal myxoma is rare. A mucinous mass of unknown etiology was observed on the left cornea of a 32-year-old male patient. We performed deep anterior lamellar keratoplasty using acellular corneal tissue and concurrent amniotic membrane transplantation. Hematoxylin and eosin staining revealed vacuolation of the parenchyma and myxoid change in the corneal tissue that occurred in the anterior half of the corneal parenchyma. We identified a myxoid stroma by Alcian blue staining and observed collagen fibers with denatured stroma by Masson trichrome staining. The patient's visual acuity improved from light perception to 20 / 200, and the intraocular pressure remained within the normal range for one year after surgery. The transplanted cornea survived successfully with well-maintained transparency, and recurrence was not observed one year after surgery.
Adult
;
*Cornea
;
Corneal Stroma/cytology/*transplantation
;
Corneal Transplantation/*methods
;
Eye Neoplasms/diagnosis/*surgery
;
Humans
;
Male
;
Myxoma/diagnosis/*surgery
8.Two Cases of Superior Limbic Keratoconjunctivitis Treated with Bevacizumab and Triamcinolone Injection.
Won Soo KIM ; Sung Wook WEE ; Jae Chan KIM
Journal of the Korean Ophthalmological Society 2014;55(3):443-448
PURPOSE: To report two cases of intractable superior limbic keratoconjunctivitis (SLK) treated with bevacizumab and triamcinolone injection. CASE SUMMARY: A 69-year-old female visited our clinic with pain in the left eye for 3 days and was diagnosed with SLK in her left eye. After 3 months of using steroid eye drops, artificial tears, and oral steroid intermittently, there was no improvement in symptoms and signs, thus this case was considered intractable with the conventional therapy. A mixture of bevacizumab (0.15 cc) and triamcinolone (0.05 cc) was injected into the sub-tenon's capsule of the left eye. After 1 week, all symptoms and signs disappeared, and there was no recurrence for 6 months. A 55-year-old female was transferred to our clinic due to SLK that did not respond to artificial tears, steroid eye drops, punctal occlusion, and botox injection for 3 months. A mixture of bevacizumab (0.15 cc) and triamcinolone (0.05 cc) was injected into the sub-tenon's capsule of the left eye. After 2 weeks, all symptoms and signs were improved, and there was no recurrence for 4 months. CONCLUSIONS: The presented 2 SLK cases are meaningful, because neovascularization disappeared and controlled inflammation was obtained following sub-tenon injection with both bevacizumab and triamcinolone.
Aged
;
Female
;
Humans
;
Inflammation
;
Keratoconjunctivitis*
;
Middle Aged
;
Ophthalmic Solutions
;
Recurrence
;
Triamcinolone*
;
Bevacizumab
9.Partial Visual Rehabilitation Using a Toric Implantable Collamer Lens in a Patient with Keratoconus: A Case Report with 20 Months of Follow-up.
Sung Wook PARK ; Mee Kum KIM ; Won Ryang WEE ; Jin Hak LEE
Korean Journal of Ophthalmology 2013;27(3):211-214
We report the case of a 37-year-old man with a high myopic keratoconus eye that was treated with a posterior chamber toric implantable collamer lens (ICL) in Korea. The patient had a history of contact lens intolerance and did not want to have a corneal transplantation. His uncorrected visual acuity (UCVA) and best spectacle corrected visual acuity were 0.02 and 0.4 in the left eye, respectively. Preoperatively, the manifest refraction was -12.0 -3.5 x 30A. Postoperatively, the manifest refraction was -1.75 x 180A. UCVA improved markedly after implantation. No intraoperative or postoperative complications were observed during 20 months of follow-up. Toric ICL implantation may be a possible alternative surgical option for the visual rehabilitation of high myopic astigmatism in keratoconus patients with rigid gas permeable contact lens intolerance and in patients who do not want to get a corneal transplant.
Adult
;
Follow-Up Studies
;
Humans
;
Keratoconus/*rehabilitation/*surgery
;
*Lens Implantation, Intraocular
;
Male
;
*Phakic Intraocular Lenses
;
*Visual Acuity
10.Effect of Age and Early Intervention with a Systemic Steroid, Intravenous Immunoglobulin or Amniotic Membrane Transplantation on the Ocular Outcomes of Patients with Stevens-Johnson Syndrome.
Kyeong Hwan KIM ; Sung Wook PARK ; Mee Kum KIM ; Won Ryang WEE
Korean Journal of Ophthalmology 2013;27(5):331-340
PURPOSE: This retrospective observational case series of fifty-one consecutive patients referred to the eye clinic with acute-stage Stevens-Johnson syndrome (SJS) or toxic epidermal necrolysis (TEN) from 1995 to 2011 examines the effect of early treatment with a systemic corticosteroid or intravenous immunoglobulin (IVIG) on the ocular outcomes in patients with SJS or TEN. METHODS: All patients were classified by age (< or =18 years vs. >18 years) and analyzed by treatment modality and early intervention with systemic corticosteroids (< or =5 days), IVIG (< or =6 days), or amniotic membrane graft transplantation (AMT) (< or =15 days). The main outcomes were best-corrected visual acuity (BCVA) in logarithm of the minimum angle of resolution (logMAR) and ocular involvement scores (OIS, 0-12), which were calculated based on the presence of superficial punctate keratitis, epithelial defect, conjunctivalization, neovascularization, corneal opacity, keratinization, hyperemia, symblepharon, trichiasis, mucocutaneous junction involvement, meibomian gland involvement, and punctal damage. RESULTS: The mean logMAR and OIS scores at the initial visit were not significantly different in the pediatric group (logMAR = 0.44, OIS = 2.76, n = 17) or the adult group (logMAR = 0.60, OIS = 2.21, n = 34). At the final follow-up, the logMAR and OIS had improved significantly in the adult group (p = 0.0002, p = 0.023, respectively), but not in the pediatric group. Early intervention with IVIG or corticosteroids significantly improved the mean BCVA and OIS in the adult group (p = 0.043 and p = 0.024, respectively for IVIG; p = 0.002 and p = 0.034, respectively for corticosteroid). AMT was found to be associated with a significantly improved BCVA or OIS in the late treatment group or the group with a better initial OIS (p = 0.043 and p = 0.043, respectively for BCVA; p = 0.042 and p = 0.041, respectively for OIS). CONCLUSIONS: Our findings suggest that patients with SJS or TEN who are aged 18 years or less have poorer ocular outcomes than older patients and that early treatment with steroid or immunoglobulin therapy improves ocular outcomes.
Acute Disease
;
Adolescent
;
Age Factors
;
Amnion/*transplantation
;
Biopsy
;
Child
;
Child, Preschool
;
Corneal Diseases/etiology/pathology/*therapy
;
Female
;
Follow-Up Studies
;
Glucocorticoids/*administration & dosage
;
Humans
;
Immunoglobulins, Intravenous/*administration & dosage
;
Infant
;
Male
;
Retrospective Studies
;
Stevens-Johnson Syndrome/complications/pathology/*therapy
;
Time Factors
;
Treatment Outcome
;
*Visual Acuity

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