1.Pediatric Idiopathic Cutaneous Pseudolymphoma of the Lower Eyelid:A Case Report
Yejin KANG ; Jaehoon SHIN ; Hoon KANG ; Jung Eun KIM
Korean Journal of Dermatology 2025;63(6):178-182
Cutaneous pseudolymphoma refers to a group of benign lymphoid proliferations that mimic cutaneous lymphomas clinically and histologically. Here, we describe a case involving a 13-year-old boy who presented with an asymptomatic, solitary, dome-shaped, skin-colored nodule on the left lower eyelid, initially suspected to be a soft fibroma or neurofibroma. Histopathological examination with immunohistochemical analysis showed a dense dermal lymphoid infiltrate predominantly composed of CD3+, CD5+ T cells, interspersed with CD20+ B cells and CD38+ plasma cells, without evidence of light chain restriction on kappa/lambda in situ hybridization. We diagnosed the lesion as cutaneous pseudolymphoma. Given the benign nature and previous unsuccessful topical treatments, we began treatment with intralesional corticosteroid therapy (triamcinolone acetonide, 5 mg/mL), resulting in significant clinical improvement within 1 month. This case underscores the importance of comprehensive histologic and immunophenotypic assessments to differentiate pseudolymphoma from early-stage cutaneous lymphomas, particularly in pediatric patients.
2.A Case of Acquired Dermal Melanocytosis of the Face and Extremities
Jaehoon HA ; Gi-Wook LEE ; Jun-Oh SHIN ; Dongyoung ROH ; Yeona KIM ; Sang-Hyeon WON ; Jungsoo LEE ; Kihyuk SHIN ; Hoonsoo KIM ; Hyun-Chang KO ; Byungsoo KIM ; Moon-Bum KIM
Korean Journal of Dermatology 2024;62(9):516-519
Acquired dermal melanocytosis, characterized by the presence of melanocytes in the dermis, varies in the timing and location of occurrence. While congenital cases, such as Mongolian spots, nevus of Ota, nevus of Ito, and blue nevus, are common, acquired cases also occur. Acquired bilateral nevus of Ota-like macules is relatively common in Asians;however, extrafacial cases, particularly those involving both the face and extremities, are extremely rare. We report the case of a 66-year-old man with symmetric pigmented patches on the scalp, face, shoulders, and dorsa of the hands for 9 months, following the onset of spots on the forehead and nose that progressively spread. Notably, nasal ala pigmentation was confirmed. Histopathological examination revealed scattered melanin-containing dendritic cells in the upper dermis. Based on the clinicopathological findings, he was diagnosed with acquired dermal melanocytosis of the face and extremities, representing a rare case.
3.A Case of Acquired Dermal Melanocytosis of the Face and Extremities
Jaehoon HA ; Gi-Wook LEE ; Jun-Oh SHIN ; Dongyoung ROH ; Yeona KIM ; Sang-Hyeon WON ; Jungsoo LEE ; Kihyuk SHIN ; Hoonsoo KIM ; Hyun-Chang KO ; Byungsoo KIM ; Moon-Bum KIM
Korean Journal of Dermatology 2024;62(9):516-519
Acquired dermal melanocytosis, characterized by the presence of melanocytes in the dermis, varies in the timing and location of occurrence. While congenital cases, such as Mongolian spots, nevus of Ota, nevus of Ito, and blue nevus, are common, acquired cases also occur. Acquired bilateral nevus of Ota-like macules is relatively common in Asians;however, extrafacial cases, particularly those involving both the face and extremities, are extremely rare. We report the case of a 66-year-old man with symmetric pigmented patches on the scalp, face, shoulders, and dorsa of the hands for 9 months, following the onset of spots on the forehead and nose that progressively spread. Notably, nasal ala pigmentation was confirmed. Histopathological examination revealed scattered melanin-containing dendritic cells in the upper dermis. Based on the clinicopathological findings, he was diagnosed with acquired dermal melanocytosis of the face and extremities, representing a rare case.
4.Successful diagnosis and treatment of recurrent atypical hemolytic uremic syndrome posttransplantation caused by the heterozygous deletion of CFH in a patient with end-stage kidney disease of uncertain etiology
Haeun LEE ; Hoon Seok KIM ; Hanbi LEE ; Sang Hun EUM ; In O SUN ; Jaehoon SHIN ; Yeong Jin CHOI ; Chul Woo YANG ; Myungshin KIM ; Byung Ha CHUNG
Kidney Research and Clinical Practice 2024;43(1):125-129
5.Dietary Habits of Newly Diagnosed Patients with Breast Cancer in Korea
Jaehoon SHIN ; Jiyeon LEE ; Yooeun YOON ; Hye Sun LEE ; Hyungmi KIM ; Yu-Jin KWON ; Ji-Won LEE
Korean Journal of Family Medicine 2024;45(3):149-156
Background:
In patients with breast cancer, a healthy diet can help reduce breast cancer-specific recurrence, mortality, and comorbid chronic disease rates. There have been few studies on dietary habits immediately after breast cancer diagnosis, especially those involving the Asian population. Therefore, this study aimed to compare the nutritional habits of newly diagnosed patients with breast cancer and the general population without cancer in Korea using propensity score (PS) matching.
Methods:
We conducted a case-controlled study of 157 patients with breast cancer and 2,363 cancer-free control participants from the Korea National Health and Nutrition Examination Survey. The PS values for the predicted probability of patients with breast cancer and the general population were estimated using logistic regression analysis, including age and body mass index. The dietary patterns were assessed using a 24-hour recall of 1 day and the Food Frequency Questionnaire.
Results:
PS matching showed that patients with breast cancer consumed fewer calories and carbohydrates; however, they consumed more protein and fat compared to the general population. Compared to the general population, patients with breast cancer consumed more healthy foods such as fish, seaweed, vegetables, fruit, mixed-grain rice, and nuts; however, they also consumed more soup, stew, and red meat.
Conclusion
Newly diagnosed patients with breast cancer have some healthy dietary habits compared to the general population. However, there is considerable room for improvement in their diet quality. Our results support the need to develop tailored dietary recommendations for patients with breast cancer during the diagnostic and posttreatment periods to improve their diet quality.
6.A Case of Acquired Dermal Melanocytosis of the Face and Extremities
Jaehoon HA ; Gi-Wook LEE ; Jun-Oh SHIN ; Dongyoung ROH ; Yeona KIM ; Sang-Hyeon WON ; Jungsoo LEE ; Kihyuk SHIN ; Hoonsoo KIM ; Hyun-Chang KO ; Byungsoo KIM ; Moon-Bum KIM
Korean Journal of Dermatology 2024;62(9):516-519
Acquired dermal melanocytosis, characterized by the presence of melanocytes in the dermis, varies in the timing and location of occurrence. While congenital cases, such as Mongolian spots, nevus of Ota, nevus of Ito, and blue nevus, are common, acquired cases also occur. Acquired bilateral nevus of Ota-like macules is relatively common in Asians;however, extrafacial cases, particularly those involving both the face and extremities, are extremely rare. We report the case of a 66-year-old man with symmetric pigmented patches on the scalp, face, shoulders, and dorsa of the hands for 9 months, following the onset of spots on the forehead and nose that progressively spread. Notably, nasal ala pigmentation was confirmed. Histopathological examination revealed scattered melanin-containing dendritic cells in the upper dermis. Based on the clinicopathological findings, he was diagnosed with acquired dermal melanocytosis of the face and extremities, representing a rare case.
7.A Case of Acquired Dermal Melanocytosis of the Face and Extremities
Jaehoon HA ; Gi-Wook LEE ; Jun-Oh SHIN ; Dongyoung ROH ; Yeona KIM ; Sang-Hyeon WON ; Jungsoo LEE ; Kihyuk SHIN ; Hoonsoo KIM ; Hyun-Chang KO ; Byungsoo KIM ; Moon-Bum KIM
Korean Journal of Dermatology 2024;62(9):516-519
Acquired dermal melanocytosis, characterized by the presence of melanocytes in the dermis, varies in the timing and location of occurrence. While congenital cases, such as Mongolian spots, nevus of Ota, nevus of Ito, and blue nevus, are common, acquired cases also occur. Acquired bilateral nevus of Ota-like macules is relatively common in Asians;however, extrafacial cases, particularly those involving both the face and extremities, are extremely rare. We report the case of a 66-year-old man with symmetric pigmented patches on the scalp, face, shoulders, and dorsa of the hands for 9 months, following the onset of spots on the forehead and nose that progressively spread. Notably, nasal ala pigmentation was confirmed. Histopathological examination revealed scattered melanin-containing dendritic cells in the upper dermis. Based on the clinicopathological findings, he was diagnosed with acquired dermal melanocytosis of the face and extremities, representing a rare case.
8.Regulation of muscle mass by microRNAs
Jaehoon SHIN ; Takayuki AKIMOTO
Japanese Journal of Physical Fitness and Sports Medicine 2023;72(5):335-341
Skeletal muscle is a vital tissue not only for maintaining posture and body movements but also for energy metabolism in human body. Skeletal muscle is highly plastic in response to various stimuli, resistance exercise or anabolic hormones can increase muscle mass, which is termed “muscle hypertrophy”. Contrary, immobility, aging and severe illness can reduce muscle mass, which is termed “muscle atrophy”. Loss of skeletal muscle mass is associated with loss of independent living, the morbidity of a variety of diseases and mortality throughout life. Therefore, understanding mechanisms that regulate skeletal muscle mass is essential for improving the quality of life. Recent studies reported microRNAs (miRNAs), which is a class of non-coding RNAs, play a crucial role in the regulation of muscle mass. This review provides a current understanding of the function of miRNAs in regulation of skeletal muscle mass.
9.Central diabetes insipidus following COVID-19 mRNA vaccination: a case report
Min-Young KIM ; Jong Ryeal HAHM ; Jaehoon JUNG ; Jung Hwa JUNG ; Kyoung Young KIM ; Hosu KIM ; Jong Ha BAEK ; Hwa Seon SHIN ; Kee Ryeon KANG ; Soo Kyoung KIM
Kosin Medical Journal 2023;38(3):219-223
The coronavirus disease 2019 (COVID-19) has been a major public health emergency worldwide. Vaccines were rapidly developed and approved to prevent the spread of viral infection. However, various side effects of the COVID-19 messenger RNA (mRNA) vaccines have been reported after their commercialization. A 24-year-old man visited our emergency department with polyuria and polydipsia that occurred after he received a COVID-19 mRNA vaccine 10 days beforehand. The initial laboratory findings showed very low urine osmolality with hyperosmolar hypernatremia. Based on these findings, diabetes insipidus was suspected, and sella magnetic resonance imaging showed an enlarged pituitary gland and the absence of posterior pituitary higher intensity. After 12 hours of using oral desmopressin acetate, urine volume decreased, and after 5 days of administration, serum electrolyte and serum osmolality improved. This case report of diabetes insipidus occurring after vaccination with the BNT162b2 mRNA COVID-19 vaccine is presented as a reminder that close monitoring is necessary for patients with polyuria and polydipsia after vaccination.
10.A sinonasal yolk sac tumor in an adult
Jaehoon SHIN ; Ji Heui KIM ; Kyeong Cheon JUNG ; Kyung-Ja CHO
Journal of Pathology and Translational Medicine 2022;56(3):152-156
Yolk sac tumors (YSTs), which are also called endodermal sinus tumors, are malignant tumors of germ cell origin. These tumors usually occur in the gonads, but 20% of cases have been reported at extragonadal sites. The head and neck is a rarely affected region that accounts for just 1% of all malignant tumors of germ cell origin. In addition, YSTs arise mostly in childhood. We present a rare pathologically pure case of primary adult YST in the sinonasal area. A 45-year-old male patient presented with a rapidly growing mass in the nasal cavity, which caused nasal obstruction and bloody post-nasal drip. The histopathologic features indicated pure YST, and immunohistochemical analysis revealed positive reactivity for Sal-like protein 4 and alpha-fetoprotein. Herein, we discuss the clinical, radiologic, and histologic features of this YST and review other cases of sinonasal YST in adults.


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