2.Syringocystadenocarcinoma Papilliferum: A Case Report and Review of the Literature
Kyoung Geun LEE ; Won CHOI ; Joon Soo LIM ; Hyung Jin HAHN ; Ki Bum MYUNG ; Seung Hyun CHEONG
Annals of Dermatology 2019;31(5):559-562
Syringocystadenocarcinoma papilliferum (SCACP) is a rare malignant adnexal neoplasm, which is considered as a malignant counterpart of syringocystadenoma papilliferum (SCAP). Clinically, SCACP appears as a nodule, inflammatory plaque, or tumor. The lesion is usually covered with crusts, which are formed by secretion of the apocrine epithelial cells. Histologically, SCACP resembles SCAP, with cystic papillomatous invaginations connected to the skin surface by funnel-shaped structures lined by infundibular epithelium. The stroma of the tumor consists of a dense inflammatory infiltrate of plasma cells and lymphocytes. SCACP differs from SCAP in terms of the architectural and cytological features of the tumor cells, and is characterized by higher nuclear cytoplasmic ratio, nuclear irregularity, coarse chromatin, and increased mitotic activity. However, the immunohistochemical findings of SCACP vary. Since only 49 cases of SCACP have been reported in the English literature, the clinical and histologic characteristics of SCACP have not been fully established. Further studies on the diagnostic criteria for SCACP are warranted. Here, we report a rare case of SCACP and present a review of other relevant literature.
Chromatin
;
Cytoplasm
;
Epithelial Cells
;
Epithelium
;
Lymphocytes
;
Plasma Cells
;
Skin
;
Sweat Gland Neoplasms
3.Does Age at Onset of First Major Depressive Episode Indicate the Subtype of Major Depressive Disorder?: The Clinical Research Center for Depression Study.
Seon Cheol PARK ; Sang Woo HAHN ; Tae Yeon HWANG ; Jae Min KIM ; Tae Youn JUN ; Min Soo LEE ; Jung Bum KIM ; Hyeon Woo YIM ; Yong Chon PARK
Yonsei Medical Journal 2014;55(6):1712-1720
PURPOSE: The purpose of this study was to evaluate the effects of age at onset of the first major depressive episode on the clinical features of individuals with major depressive disorder (MDD) in a large cohort of Korean depressed patients. MATERIALS AND METHODS: We recruited 419 MDD patients of age over 18 years from the Clinical Research Center for Depression study in South Korea. At the start of the study, the onset age of the first major depressive episode was self-reported by the subjects. The subjects were divided into four age-at-onset subgroups: childhood and adolescent onset (ages <18), early adult onset (ages 18-44), middle adult onset (ages 45-59), and late onset (ages 60+). Using analysis of covariance (ANCOVA) and ordinal logistic regression analysis with adjusting the effect of age, the relationships between clinical features and age at onset of MDD were evaluated. RESULTS: There was an apparent, but inconsistent correlation between clinical features and age at onset. Earlier onset MDD was significantly associated with higher proportion of female gender [adjusted odds ratio (AOR)=0.570, p=0.022], more previous suicide attempts (AOR=0.635, p=0.038), greater number of previous depressive episodes (F=3.475, p=0.016) and higher scores on the brief psychiatric rating scale (F=3.254, p=0.022), its negative symptom subscale (F=6.082, p<0.0001), and the alcohol use disorder identification test (F=7.061, p<0.0001). CONCLUSION: Early age at onset may increase the likelihood of distinguishable MDD subtype, and age at onset of the first major depressive episode is a promising clinical indicator for the clinical presentation, course, and outcome of MDD.
Adolescent
;
Adult
;
Age Distribution
;
Age of Onset
;
Aged
;
Depression/epidemiology
;
Depressive Disorder, Major/*classification/*diagnosis/psychology
;
Female
;
Humans
;
Life Change Events
;
Male
;
Middle Aged
;
Odds Ratio
;
Psychiatric Status Rating Scales
;
Regression Analysis
;
Republic of Korea
;
Suicide, Attempted/psychology
;
Young Adult
4.Recombinant DNA and Protein Vaccines for Foot-and-mouth Disease Induce Humoral and Cellular Immune Responses in Mice.
Ji young BAE ; Sun Hwa MOON ; Jung Ah CHOI ; Jong Sug PARK ; Bum Soo HAHN ; Ki Yong KIM ; Byunghan KIM ; Jae Young SONG ; Dae Hyuck KWON ; Suk Chan LEE ; Jong Bum KIM ; Joo Sung YANG
Immune Network 2009;9(6):265-273
BACKGROUND: Foot-and-mouth disease virus (FMDV) is a small single-stranded RNA virus which belongs to the family Picornaviridae, genus Apthovirus. It is a principal cause of FMD which is highly contagious in livestock. In a wild type virus infection, infected animals usually elicit antibodies against structural and non-structural protein of FMDV. A structural protein, VP1, is involved in neutralization of virus particle, and has both B and T cell epitopes. A RNA-dependent RNA polymerase, 3D, is highly conserved among other serotypes and strongly immunogenic, therefore, we selected VP1 and 3D as vaccine targets. METHODS: VP1 and 3D genes were codon-optimized to enhance protein expression level and cloned into mammalian expression vector. To produce recombinant protein, VP1 and 3D genes were also cloned into pET vector. The VP1 and 3D DNA or proteins were co-immunized into 5 weeks old BALB/C mice. RESULTS: Antigen-specific serum antibody (Ab) responses were detected by Ab ELISA. Cellular immune response against VP1 and 3D was confirmed by ELISpot assay. CONCLUSION: The results showed that all DNA- and protein-immunized groups induced cellular immune responses, suggesting that both DNA and recombinant protein vaccine administration efficiently induced Ag-specific humoral and cellular immune responses.
Animals
;
Antibodies
;
Clone Cells
;
DNA
;
DNA, Recombinant
;
Enzyme-Linked Immunosorbent Assay
;
Enzyme-Linked Immunospot Assay
;
Epitopes, T-Lymphocyte
;
Foot-and-Mouth Disease
;
Foot-and-Mouth Disease Virus
;
Humans
;
Immunity, Cellular
;
Livestock
;
Mice
;
Picornaviridae
;
Proteins
;
RNA Replicase
;
RNA Viruses
;
Vaccines
;
Virion
;
Viruses
5.CT and MR Findings of Neurological Disorders Associated with Pregnancy and Childbirth.
Jee Young KIM ; Kook Jin AHN ; Young Joo KIM ; Bum Soo KIM ; Seong Tae HAHN
Journal of the Korean Radiological Society 2008;59(2):65-73
The onset of pregnancy may predispose women to a variety of neurological diseases due to changes in their hemodynamics, hormonal effects, and complications associated with childbirth. The spectrum of neurological disorders associated with pregnancy and childbirth include hypertensive intracerebral hemorrhaging, posterior reversible encephalopathy syndrome (PRES) (secondary to eclampsia), Wernicke encephalopathy, cerebral venous sinus thrombosis, Sheehan's syndrome, hypoxic ischemic encephalopathy (secondary to pulmonary amniotic fluid embolism), multifocal infarctions, and extra-potine myelinolysis. The recognition of the various imaging findings of these diseases, along with the clinical presentations, should aid in their early diagnosis and prompt treatment. The purpose of this pictorial assay is to describe the characteristic CT and MR findings of these diseases with a literature review to explain the mechanisms and clinical symptoms.
Amniotic Fluid
;
Brain
;
Early Diagnosis
;
Female
;
Hemodynamics
;
Humans
;
Hypopituitarism
;
Hypoxia-Ischemia, Brain
;
Infarction
;
Nervous System Diseases
;
Parturition
;
Pregnancy
;
Pregnancy Complications
;
Sinus Thrombosis, Intracranial
;
Tomography, X-Ray Computed
;
Wernicke Encephalopathy
6.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
;
Conjunctival Neoplasms/radiography
;
Cysts/radiography
;
Eye Neoplasms/*radiography
;
Hemangiopericytoma/radiography
;
Humans
;
Lacrimal Apparatus/*pathology
;
Lacrimal Apparatus Diseases/radiography
;
Lipoma/radiography
;
Lymphoma/radiography
;
Neoplasms, Glandular and Epithelial/radiography
;
Neurofibroma/radiography
;
Sarcoma, Myeloid/radiography
7.Imaging Findings of Central Nervous System Vasculitis Associated with Goodpasture's Syndrome: a Case Report.
Jee Young KIM ; Kook Jin AHN ; Jung Im JUNG ; So Lyung JUNG ; Bum Soo KIM ; Seong Tae HAHN
Korean Journal of Radiology 2007;8(6):545-547
Glomerulonephritis and pulmonary hemorrhage are features of Goodpasture's syndrome. Goodpasture's syndrome accompanied with central nervous system (CNS) vasculitis is extremely rare. Herein, we report a rare case of CNS vasculitis associated with Goodpasture's syndrome in a 34-year-old man, who presented with a seizure and sudden onset of right sided weakness. He also had recurrent hemoptysis of one month's duration. Goodpasture's syndrome is histologically diagnosed by intense linear deposits of IgG along the glomerular basement membrane in both renal and lung tissues.
Adult
;
Anti-Glomerular Basement Membrane Disease/complications/*diagnosis/therapy
;
Anti-Inflammatory Agents/administration & dosage
;
Brain/*pathology
;
Contrast Media/administration & dosage
;
Diagnosis, Differential
;
Fluorescent Antibody Technique
;
Hemoptysis/etiology
;
Humans
;
Image Enhancement/methods
;
Immunoglobulin G/immunology
;
Kidney/ultrasonography
;
Lung/pathology/*radiography
;
Magnetic Resonance Imaging
;
Male
;
Methylprednisolone/administration & dosage
;
Muscle Weakness/etiology
;
Plasmapheresis
;
Rare Diseases
;
Seizures/etiology
;
Tomography, X-Ray Computed
;
Vasculitis, Central Nervous System/*diagnosis/etiology/therapy
8.An Analysis of the Ultrasound Findings of False Negative Cases for an Initial Ultrasound-guided Fine Needle Aspiration Biopsy (FNAB).
Jee Young KIM ; So Lyung JUNG ; Bum Soo KIM ; Kook Jin AHN ; Seong Tae HAHN
Journal of the Korean Radiological Society 2007;57(3):213-218
PURPOSE: To analyze the ultrasonographic (US) findings of thyroid nodules that yielded false negative results after an initial ultrasound-guided fine needle aspiration biopsy (FNAB). MATERIALS AND METHODS: Between August 2003 and February 2006, 389 patients with 405 thyroid nodules received a repeat US-guided FNAB. We retrospectively reviewed the US findings, cytology results and postsurgical pathological results. The cytology diagnoses were classified as benign, a suspicious malignancy, a follicular neoplasm, a papillary carcinoma, and a non-diagnostic result. The US findings of the thyroid nodules were analyzed with regard to size, internal content, shape, margin, echogenecity, and calcification pattern. RESULTS: Of the 405 thyroid nodules, 17 nodules were false negative. The major US findings of these nodules were a solid internal component in 16 nodules, hypoechogenicity or marked hypoechogenicity in 14 nodules, microcalcifications in 12 nodules, an ovoid to round shape in 9 nodules and a well-defined smooth margin in 9 nodules. CONCLUSION: An repeat US-guided FNAB should be performed if the thyroid nodules have one of the malignant US features such as hypoechogenecity or marked hypoechogenecity, a microcalcification, a taller than wide shape or a well-defined spiculate margin although the cytology results indicated a benign lesion. In addition, thyroid nodules with findings of a well-defined smooth margin, ovoid to round shape, and solid internal component might also be subject to a repeat US-guided FNAB to exclude a malignancy.
Biopsy*
;
Biopsy, Fine-Needle*
;
Carcinoma, Papillary
;
Diagnosis
;
Humans
;
Retrospective Studies
;
Thyroid Diseases
;
Thyroid Nodule
;
Ultrasonography*
9.Epidemiology of Infectious Keratitis(II): A Multi-center Study.
Young Ho HAHN ; Tae Won HAHN ; Hungwon TCHAH ; Si Hwan CHOI ; Kee Yong CHOI ; Ki San KIM ; Won Ryang WEE ; Jae Duck KIM ; Hyo Myung KIM ; Jang Hyun CHUNG ; Ha Bum LEE ; Jae Chan KIM ; Kyung Hyun JIN ; Young Su YUN ; Yoon Won MYONG ; Sung Kun CHUNG ; Choun Ki JOO ; Man Soo KIM ; Myung Kyoo KO ; Eung Kweon KIM ; Jong Hyuck LEE ; Hyung Jun KIM ; Gi Bong KIM ; Beoum Jin CHO ; Woo Jung KIM ; Woo Chan PARK ; Jin Hak LEE
Journal of the Korean Ophthalmological Society 2001;42(2):247-265
To identify risk factors and causative organisms, and to evaluate clinical manifestations, methods and results of treatment in infectious keratitis, an epidemiological study was performed prospectively under the identical protocol from April 1995 to March 2000.Logistic regression analysis was used to evaluate possible risk factors. The 1474 cases of infectious keratitis reported from 22 hospitals were studied. Five hundred forty-four organisms(442 bacteria, 82 fungi, 20 A c a n t h a m o e b a)were detected in 1320 eyes with infectious keratitis excluding 154 herpetic keratitis. The Pseudomonas aeruginosa was the most common organism in bacterial keratitis, and Fusariumspp. was the major isolate in fungal keratitis. Contact lens wear and occupation(industry, forester, miner, fisherman)were the risk factors for bacterial keratitis. Risk factors in fungal keratitis were fifth decade of age, farmer, and systemic diseases(diabetes mellitus etc.). Risk factors in herpetic keratitis were male and occupation(office worker, service, student, housewife). Risk factors in Acanthamoeba keratitis was contact lens wear.
Acanthamoeba Keratitis
;
Bacteria
;
Epidemiologic Studies
;
Epidemiology*
;
Fungi
;
Humans
;
Keratitis
;
Keratitis, Herpetic
;
Male
;
Prospective Studies
;
Pseudomonas aeruginosa
;
Risk Factors
10.Two Cases of Malignant Lymphoma Involving Bilateral Adrenal Glands as Huge Masses.
Seung Hyeok HAN ; Jin Seok KIM ; Myung Soo KIM ; Hye Won CHUNG ; Jae Ho JUNG ; Young Suck GOO ; Chul Woo AHN ; Jae Hyun NAM ; Sang Soo JUNG ; Young Duk SONG ; Sung Kil LIM ; Kyung Rae KIM ; Hyun Chul LEE ; Kap Bum HUH ; Jee Sook HAHN
Journal of Korean Society of Endocrinology 2000;15(1):121-127
Adrenal gland is a common site of metastatic tumors such as breast cancer, lung cancer, and colon cancer. When adrenal mass is found incidentally, adenoma is the most common among single adrenal masses. But in the case of bilateral adrenal masses, infection, bilateral metastases and hemorrhage are common. Secondary involvement of the adrenal gland is found in 25% of autopsy cases of non-Hodgkin's lymphoma. However, adrenal insufficiency is rare because it becomes apparent only when approximately 90% of adrenal cortex is destructed. We exprienced two cases of malignant lymphoma which involved the adrenal glands bilaterally. One case in which adrenal insufficiency was suspicious, was accompanied by hypovolemic shock and sepsis at the initial presentation. He died of sepsis combined with DIC even though hydrocortisone, intravenous saline infusion, and antibiotics therapy were started immediately. The other one was found incidentally, in which adrenal infiltraion was confirmed by CT scan. Hormonal level was normal and adrenal masses disappeared after chemotherapy.
Adenoma
;
Adrenal Cortex
;
Adrenal Glands*
;
Adrenal Insufficiency
;
Anti-Bacterial Agents
;
Autopsy
;
Breast Neoplasms
;
Colonic Neoplasms
;
Dacarbazine
;
Drug Therapy
;
Hemorrhage
;
Hydrocortisone
;
Lung Neoplasms
;
Lymphoma*
;
Lymphoma, Non-Hodgkin
;
Neoplasm Metastasis
;
Sepsis
;
Shock
;
Tomography, X-Ray Computed

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