• 한국임상수의학회지
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• 제19권3호
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• pp.337-341
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• 2002

In 2001, eight small-sized dogs and three medium-sized dogs with or without clinical signs such as vomiting, dyspnea and enlargement of superficial lymph nodes were diagnosed as lymphoma by radiography, ultrasonography and cytology. Among them, six were female mainly over 7 years old and others were male around 4 years old. There were six cases of multicentric form lymphoma, three cases of mediastinal form, an alimentary and an extranodal form, respectively. Radiographic findings were enlarged cranial mediastinal lymph node, sternal lymph node, and tracheobronchial lymph nodes on thorax and hepatomegaly, splenomegaly, and enlarged sublumbar lymph nodes on abdomen. Ultrasonographic findings revealed enlarged abdominal lymph nodes and multifocal hypoechoic lesions on the liver. Especially, severe wall thickness of small bowel was observed in a dog with alimentary lymphoma. Three dogs were dead during chemotherapy, and three dogs were dead without any treatment. Three dogs did not return and two treated dog showed normal status. Radiography and ultrasonography, although not giving an final diagnosis for lymphoma, are useful for assessment and diagnosis of lymphoma.

• Animal Systematics, Evolution and Diversity
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• 제37권4호
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• pp.358-361
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• 2021

The genus Rhopalaea Philippi, 1843 is firstly recorded as a Korean fauna. It is distinct from other genera of Diazonidae in order Aplousobranchia by having solitary individuals or at most two embedded in a common test. Solitary ascidian, Rhopalaea crassa (Herdman, 1880), is also newly reported from Korean waters. Rhopalaea crassa has a club-shaped body, developed thorax, a vertical gut loop and yellow patches in transparent test. Specimens of R. crassa examined in this study were collected from the subtidal zone of Jeju-do Island by scuba diving. In this paper, detailed descriptions and photographs of specimens and living forms of R. crassa are provided.

• Journal of Interdisciplinary Genomics
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• 제3권2호
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• pp.30-34
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• 2021

Campomelic dysplasia (CD) is a rare genetic disorder characterized by multiple skeletal anomalies and the abnormal development of male reproductive organs. To date, the SOX9 gene is the only known causal gene for CD, and approximately 90 causative mutations in SOX9 have been identified worldwide. CD is diagnosed based on clinical characteristics of skeletal dysplasia (e.g., short bowed long bones, kyphoscoliosis, bell-shaped thoracic cage with 11 pairs of ribs, and hypoplastic scapulars), typical facial features of Pierre Robin sequence with cleft palate, and gonadal dysgenesis in 46,XY individuals. Most patients with CD exhibit life-threatening respiratory failure owing to laryngotracheomalacia and hypoplastic thorax during the neonatal period. Although fatal complications decrease after infancy, several medical conditions continue to require proper management. A better understanding of this rare but lethal condition may lead to more appropriate treatments for patients.

• Journal of Chest Surgery
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• 제52권1호
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• pp.44-46
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• 2019

Gorham-Stout disease (GSD) was first described by Gorham and colleagues in 1954, but its precise mechanism and cause remain to be elucidated. In this condition, voluminous and potentially fatal chylous effusions into the thorax can occur. Herein, we describe a case of GSD in which the patient presented with massive pleural effusions and mottled osteolytic bone lesions. We performed multiple operations, including thoracic duct ligation using video-assisted thoracoscopic surgery and thoracotomic decortication, but these procedures did not succeed in preventing recurrent pleural effusion and chest wall lymphedema. After administering sirolimus ($0.8mg/m^2$, twice a day) and propranolol (40 mg, twice a day), the process of GSD in this patient has been controlled for more than 2 years.

• Journal of Genetic Medicine
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• 제16권1호
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• pp.27-30
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• 2019

Smith-Kingsmore syndrome (SKS; OMIM 616638), also known as macrocephaly-intellectual disability-neurodevelopmental disorder-small thorax syndrome (MINDS; ORPHA 457485), is a rare autosomal dominant disorder, the prevalence of which is not known. It is caused by a heterozygous germline mutation in MTOR (OMIM 601231). Ten different MTOR germline mutations in 27 individuals have been reported in the medical literature to date. These were all gain-of-function missense variants, and about half of the 27 individuals had c.5395G>A p.(Glu1799Lys) in MTOR. Here, I report for the first time a Korean patient with the heterozygous germline mutation c.5395G>A p.(Glu1799Lys) in MTOR. It was found to be a de novo mutation, which was identified by whole-exome sequencing and confirmed by Sanger sequencing. The patient showed typical clinical features of SKS, including macrocephaly/megalencephaly; moderate intellectual disability; seizures; behavioral problems; and facial dysmorphic features of curly hair, frontal bossing, midface hypoplasia, and hypertelorism.

• Archives of Plastic Surgery
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• 제46권3호
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• pp.262-266
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• 2019

Transsexual individuals with gender dysphoria or gender identity disorder are rare, with a prevalence reported to range from 0.002% to 0.014%. Studies have shown that mastectomy yields significant improvements in body image and self-esteem in female-to-male transsexual patients. In patients with grade III breast ptosis, mastectomy with a nipple-areolar complex (NAC) graft is the most commonly used technique, although it has several disadvantages. In the case described herein, a bilateral mastectomy preserving the NAC in an inferior pedicle was performed. Additionally, a thin superior thoracic dermal-fat flap was preserved and eventually sutured at the previous inframammary fold, preventing an inverted T scar. This case shows the advantage of this technique for preserving the blood supply and innervation of the NAC, with a low hypopigmentation risk. Furthermore, in this technique, the patch effect does not impair the results of the NAC graft, and there is no need to use an inverted T scar that may result in thoracic feminization.

• Journal of Species Research
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• 제8권1호
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• pp.1-96
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• 2019

The suborder Symphyta comprises more than 8,000 described species worldwide, of which about 4,400 extant species are recorded from the Eastern Palaearctic. Symphyta can be easily distinguished from the suborder Apocrita by the abdomen, which is broadly joined to the thorax. The larvae of most species feed on herbaceous to woody. A list of the 418 described species of Symphyta in Korea is presented. The list is in taxonomic sequence by superfamily, family, subfamily and genus and includes 116 genera in 22 subfamilies, 12 families, and seven superfamilies. We provide the page reference of the original description of every species and genus listed, Korean name, host records, and all Korean records. The list also provides the distribution of all the species by country.

• Animal Systematics, Evolution and Diversity
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• 제37권1호
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• pp.64-69
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• 2021

The genus Krenosmittia is a small group of Orthocladiinae, containing a total of twenty species in the world. Among them, six species were found in Japan, four species in China, and five species from the Russian Far East. This genus can be distinguished from other Orthocladiinae genera by the eyes bare, absence of acrostichals on thorax, costa strongly extended, anal vein ending proximal to FCu, squama bare, and having a strongly developed virga. We report three new species: K. danyangensis n. sp., K. triangulia n. sp., and K. pseudoannulata. The genus Krenosmittia is the first record in Korea. Line drawings of the diagnostic characters are provided for all the species recognized in this study.

• Animal Systematics, Evolution and Diversity
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• 제37권1호
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• pp.70-77
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• 2021

The genus Parorthocladius is a small group among the subfamily Orthocladiinae (Diptera: Chironomidae). A total of ten species of Parorthocladius have been recorded in the world, of which two species were found from Japan, three species from China, and three species from the Russian Far East. Only one species, P. nudipennis is widely distributed in Europe and the Russian Far East. This genus can be distinguished from other genera by the absence of acrostichals on the thorax, wing vein R4+5 ending proximal to the tip of vein M3+4, anal point parallel side, rounded apically. We report four new species of Parorthocladius collected in Korea and described them with illustrations. As a result, fourteen species of Parorthocladius have been recorded in the world.

• 한국임상수의학회지
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• 제39권2호
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• pp.87-92
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• 2022

A 14-year-old castrated male Persian cat presented with a 2-week history of respiratory difficulty. On physical examination, the patient showed intermittent open-mouth breathing and thoracic auscultation revealed wheezing. Thoracic radiographs revealed a narrowed upper airway and pulmonary infiltration. Computed tomography detected a mass occluding the lumen of the trachea at the level of the entrance to the thorax, a mass causing right main bronchus stenosis, and a nodule on the right caudal lung lobe. Bronchoalveolar lavage cytology tentatively diagnosed a carcinoma. Tracheal mass resection was performed through tracheostomy. Histopathology confirmed the presence of tracheobronchial carcinoma. The survival time after diagnosis was 10 months, during which time the cat underwent tracheostomy, debulking by endotracheal tube, and tracheal stent placement procedures in combination with toceranib phosphate adjuvant chemotherapy.