• 제목/요약/키워드: Uncommon complications

검색결과 161건 처리시간 0.024초

Schwannoma on the nasal dorsum and tip with sensory changes

  • Yoon, Sung Ho;Kim, Cha Soo;Oh, Jae Wook;Lee, Keun Cheol
    • 대한두개안면성형외과학회지
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    • 제21권6호
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    • pp.380-383
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    • 2020
  • Schwannomas, which originate from Schwann cells in the peripheral nervous system, are slowg-rowing and uncommon benign tumors. Most schwannomas (90%) occur in isolation, and multiple occurrences are a characteristic feature of neurofibromas. Schwannomas of the nose and nasal tip are particularly unusual. Although a few cases of schwannomas of the sinusoidal tract and nasal septum have been reported, schwannomas arising from the nasal dorsum area and tip are extremely rare. Sensory abnormalities are also a very rare symptom. We excised a schwannoma on the nasal dorsum through direct incision and a schwannoma on the nasal tip through open rhinoplasty. No postoperative complications involving recurrence, hematoma, or infection occurred. The possibility of neurological changes should be considered in cases of an abnormality in the peripheral nervous system. Schwannoma must be kept in mind as a possible cause of neurological changes localized to a specific dermatome, and should always be considered in the differential diagnosis of a mass on the nose.

Idiopathic multicentric Castleman disease presenting progressive reticular honeycomb infiltration of lung and immunoglobulin G and immunoglobulin G4 dominant hypergammaglobulinemia: a case report

  • Kim, Hyun-Je;Hong, Young-Hoon
    • Journal of Yeungnam Medical Science
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    • 제39권2호
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    • pp.153-160
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    • 2022
  • Multicentric Castleman disease (MCD) is an uncommon systemic lymphoproliferative disorder that may cause multiple organ damage. Castleman disease-associated diffuse parenchymal lung disease (DPLD) has not been well studied. A 32-year-old man was referred to our hospital for progressive generalized weakness, light-headedness, and dyspnea on exertion for more than one year. Laboratory evaluations showed profound anemia, an elevated erythrocyte sedimentation rate, and an increased C-reactive protein level with polyclonal hypergammaglobulinemia. Chest radiography, computed tomography (CT), and positron emission tomography-CT scan demonstrated diffuse lung infiltration with multiple cystic lesions and multiple lymphadenopathy. In addition to these clinical laboratory findings, bone marrow, lung, and lymph node biopsies confirmed the diagnosis of idiopathic MCD (iMCD). Siltuximab, an interleukin-6 inhibitor, and glucocorticoid therapy were initiated. The patient has been tolerating the treatment well and had no disease progression or any complications in 4 years. Herein, we report this case of human herpesvirus-8-negative iMCD-associated DPLD accompanied by multiple cystic lesions, multiple lymphadenopathy, and polyclonal hypergammaglobulinemia with elevated immunoglobulin G (IgG) and IgG4 levels. We recommend a close evaluation of MCD in cases of DPLD with hypergammaglobulinemia.

Pleuroperitoneal communication-associated pleuritis as an uncommon cause of fever of unknown origin in a child on peritoneal dialysis: a case report

  • Juhee Park;Heeyon Yoon;Jiwon Jung;Jina Lee;Joo Hoon Lee
    • Childhood Kidney Diseases
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    • 제27권1호
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    • pp.46-53
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    • 2023
  • Pleuroperitoneal communication (PPC) is a rare mechanical complication of peritoneal dialysis (PD), which causes dialysate to move from the peritoneal cavity to the pleural cavity, resulting in pleural effusion. Typically, PPC is discovered through pleural effusion in PD patients who are not in volume overload status. A unique characteristic of the pleural effusion caused by PPC is that it is not resolved by increasing ultrafiltration by dialysis. In this report, we present a 7-year-old girl with PD after birth with the history of various infectious PD-related complications, presenting with fever ongoing for 6 months. PPC-associated pleuritis was suspected as the cause of fever, which eventually developed after long-term PD and induced complicated pleural effusion, lung inflammation, and prolonged fever for 6 months.

Asymptomatic Uterine Rupture Caused by Trauma in a Small-Sized Non-Gravid Dog

  • Ye-Eun Kim;Sang-Hyun Nam;Won-Jong Lee;Chang-Hwan Moon;Geum-Lan Hong;Ju-Young Jung;Jae-Min Jeong;Hae-Beom Lee;Seong-Mok Jeong;Dae-Hyun Kim
    • 한국임상수의학회지
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    • 제41권2호
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    • pp.112-116
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    • 2024
  • Uterine rupture is uncommon in small animals and can be caused by trauma, infection, dead fetus, or inappropriate obstetric techniques. A 4-year-old, intact female mixed-breed dog weighing 3 kg presented for elective ovariohysterectomy with a history of a motor vehicle accident two months previously. The patient showed no clinical signs of uterine abnormalities or evidence of pregnancy during physical examination. Clinical examinations, radiography, and ultrasonography revealed no significant findings. During ovariohysterectomy, a completely transected left uterine horn and dome-shaped ends were identified. The uterine layers were everted such that the endometrium could be seen outside the uterine horn. The dog recovered without post-operative complications and was discharged the following day. This report describes a rare case of an asymptomatic uterine rupture caused by trauma in a non-gravid dog.

A Case Report of Prolonged Hemorrhage Following Traditional Phlebotomy (Fasd)

  • Sajjad Sadeghi
    • 대한약침학회지
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    • 제27권1호
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    • pp.47-52
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    • 2024
  • Phlebotomy, a therapeutic method of bloodletting typically performed using a needle, has a traditional technique known as "Fasd." In this method, blood is extracted by creating a longitudinal incision on a vein (3-5 mm) with a surgical scalpel blade, usually blade No. 11. Due to the incision in the vessel wall, establishing hemostasis is more challenging compared to conventional methods. Hemostasis is usually achieved within minutes after Fasd. We present a case highlighting an uncommon yet significant complication of traditional phlebotomy. A 55-year-old man with no prior medical conditions underwent traditional phlebotomy at an academic traditional medicine clinic. Senior MD-PhD students in Iranian Traditional Medicine, under professor supervision, performed Fasd. A sterile scalpel blade No. 11 was used to create a longitudinal incision of approximately 4 mm on the patient's median basilic vein in the right hand. After removing 400 cc of blood, a pressure dressing was applied to the incision site. Despite attempts such as hand elevation, ice pack application, prolonged direct pressure, and tight elastic bandaging, bleeding from the incision persisted. After an hour of supportive therapy, hemostasis was eventually achieved within a few minutes using burnt cotton dressing (a traditional method for blood hemostasis). Following intravenous hydration, the patient was discharged in stable condition and reported no issues during the one-month follow-up. The traditional phlebotomy (Fasd) carries the risk of serious complications, including uncontrolled and prolonged bleeding. Further research on the efficacy and safety of burnt cotton dressing for controlling hemostasis is recommended.

자연성 종격동 기종: 두 병원에서의 임상 경험 24예 (Spontaneous Pneumomediastinum: Clinical Experience of 24 Patients in Two Medical Center)

  • 문현종
    • Journal of Chest Surgery
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    • 제43권6호
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    • pp.663-668
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    • 2010
  • 배경: 자연성 종격동 기종은 드문 질환으로 세계적으로 보고된 환자도 적다. 주로 젊은 남자에서 발병하며 양성의 자연 치유 경과의 질환으로 어떤 특별한 이유 없이 일어난다. 폐기포 파열을 일으키는 흉강내 압력 변화 이후 나타나게 된다. 두 병원의 임상 경험을 분석하여 적정한 치료에 도움이 되고자 한다. 대상 및 방법: 후향적으로 2003년 3월부터 2010년 8월까지 자연성 종격동 기종 환자들을 연구하였다. 결과: 24명의 환자가 자연성 종격동 기종으로 진단되었다. 이들 24명의 환자는 18명의 남자와 6명의 여자로 구성되었고, 평균 나이는 18.9세였다(범위 10~33살). 초기 주요 증상은 흉부 통증(79.2%), 이후 통증(62.5%), 피하 기종(4 1.7%)이었고 유발 인자로 운동(16.7%), 기침(12.5%), 구토(12.5%) 등이었고 유발 인자가 없는 경우가 54.2%였다. 모든 환자에서 흉부 단순 촬영과 단층 촬영이 이루어졌으며, 25% 환자에서 진단을 위해 단층 촬영이 필요하였다. 백혈구 수치와 C반응 단백(CRP)가 측정되었는데 초기 평균 수치는 각각 $9,790{\pm}3,240/{\mu}L$$1.31{\pm}1.71mg/dL$, 최종 평균 수치는 $5,440{\pm}1,665/{\mu}L$$0.72{\pm}0.73mg/dL$이었다. 23명의 환자가 입원하였으며(평균 $5.0{\pm}1.8$일) 증상은 자연 치유되었으며 합병증은 없었다. 결론: 자연성 종격동 기종은 약한 염증성 증세를 보이는 양성 질환이며 종종 흉부 또는 인후 통증을 나타낸다. 바람직하지 못한 결과를 방지하기 위하여 비침습적인 검사로 이차성 원인이 배제되어야 한다. 합병증과 재발이 거의 없는 관계로 증상에 따라 외래 진료나 단기적인 입원이 합당하다고 하겠다.

췌십이지장 손상에서의 응급췌십이지장절제술 (Emergency Pancreaticoduodenectomy for Severe Pancreaticoduodenal Injury)

  • 박인규;황윤진;권형준;윤경진;김상걸;천재민;박진영;윤영국
    • Journal of Trauma and Injury
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    • 제25권4호
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    • pp.115-121
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    • 2012
  • Purpose: Severe pancreaticoduodenal injuries are relatively uncommon, but may result in high morbidity and mortality, especially when management is not optimal, and determining the appropriate treatment is often difficult. The objective of this study was to review our experience and to evaluate the role of a pancreaticoduodenectomy (PD) in treatment of pancreaticoduodenal injuries. Methods: We performed a retrospective review of 16 patients who underwent an emergency PD at our hospital for severe pancreaticoduodenal injury from 1990 to 2011. Demographic data, clinical manifestations, mechanism and severity of the injury, associated injuries, postoperative complications and outcomes were reviewed. Results: The mean age of the 16 patients was $45{\pm}12years$ ($mean{\pm}standard$ deviation), and 15(93.8%) patients were male. All patients underwent an explorative laparotomy after a diagnosis using abdominal computed tomography. Almost all patients were classified as AAST grade higher than III. Thirteen(83.3%) of the 16 patients presented with blunt injuries; none presented with a penetrating injury. Only one(6.3%) patients had a combined major vascular injury. Fifteen patients underwent a standard Whipple's operation, and 1 patient underwent a pylorus-preserving pancreaticoduodenectomy. Two of the 16 patients required an initial damage-control procedure; then, a PD was performed. The most common associated injured organs were the small bowel mesentery(12, 75%) and the liver(7, 43.8%). Complications were intraabdominal abscess(50%), delayed gastric emptying(37.5%), postoperative pancreatic fistula(31.5%), and postoperative hemorrhage (12.5%). No mortalities occurred after the PD. Conclusion: Although the postoperative morbidity rate is relatively higher, an emergency PD can be perform safely without mortality for severe pancreaticoduodenal injuries. Therefore, an emergency PD should be considered as a life-saving procedure applicable to patients with unreconstructable pancreaticoduodenal injuries, provided that is performed by an experienced hepatobiliary surgeon and the patient is hemodynamically stable.

둔상에 의한 기관 완전 절단 - 1예 보고 - (Complete Transsection of the Trachea by Blunt Trauma)

  • 김대환;유병하;김한용;황상원
    • Journal of Chest Surgery
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    • 제40권1호
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    • pp.79-82
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    • 2007
  • 둔상에 의한 기관-기관지 파열은 발생빈도가 낮은 질환이나, 점차 그 빈도가 증가하는 추세이다. 일단 기관-기관지 파열이 발생하면 매우 심각한 증상을 유발하여 생명의 위협을 초래하고, 많은 합병증을 야기하기 때문에 조기에 진단하여 외과적으로 치료하는 것이 바람직하다 본 저자들은 35세의 남자 환자에서 교통사고 후 발생한 기관 완전 절단의 한 예를 보고하는 바이다. 환자는 수상 후 심한 호흡곤란과 경부, 전흉부에 생긴 피하기종을 주소로 내원하여 양측 긴장성 기흉 진단하에 응급 흉관 삽관술 시행 후에도 대량의 공기 유출이 지속되었고, 피하기종은 복부와 음낭까지 진행되었으며, 호흡부전은 더욱 심화되어 기관-기관지 파열이 강력히 의심되어 응급 수술을 시행하였다. 수술실에서 시행한 술 전 기관지내시경상 성대 하에서 기관의 횡단 절단을 확인하였으며, 수술은 목에 칼라 절개를 가한 후 절단된 기관을 확인하여 4-0 바이크릴(Vicryl) 봉합사를 이용하여 단속봉합에 의한 단단 문합술을 시행하였다. 술 후 흉관을 통한 공기유출은 없었고 기관지내시경 추적 검사상 양호한 소견을 보였으며 특별한 합병증 발병 없이 퇴원하였다.

간헐적 복통과 오심, 구토로 내원한 Trichobezoar 1례 (A Case of Trichobezoar in a Child Who Visited with Intermittent Abdominal Pain, Nausea and Vomiting)

  • 안승인;유정석;오경창;김봉림;김성섭;김연호;장진근
    • Clinical and Experimental Pediatrics
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    • 제48권4호
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    • pp.433-437
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    • 2005
  • 위석은 비교적 흔하지 않은 질환이지만, 진단을 못할 경우 위궤양과 출혈, 장천공, 장중첩증, 장폐쇄, 복막염 등의 심각한 합병증을 동반할 수 있는 만성적 복통의 한 원인이며, 모발석 환아의 대부분은 발모벽과 식모증의 과거력이 있다. 저자들은 내원 4년 전까지 자기 머리카락을 뽑아서 먹는 습관이 있었고, 이후 간헐적 복통과 오심, 구토를 일으킨 11세 여아에서 모발석을 경험하였기에 문헌 고찰과 함께 보고하는 바이다.

A Rare Case of Pulmonary Epithelioid Hemangioendothelioma Presenting with Skin Metastasis

  • Ro, Hyung-Suk;Shin, Jin Yong;Roh, Si-Gyun;Lee, Nae-Ho;Yang, Kyung-Moo;Moon, Woo-Sung
    • Archives of Plastic Surgery
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    • 제43권3호
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    • pp.284-287
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    • 2016
  • Epithelioid hemangioendothelioma (EHE) is a well-differentiated and rare vascular tumor. Systemic metastases are uncommon. Herein, we present a patient with skin metastasis of pulmonary EHE (PEH) that was treated by wide excision. A 76-year-old male was evaluated due to pulmonary thromboembolism and a solitary pulmonary nodule. A biopsy was performed and pathological examination of the mass confirmed EHE. No metastasis was observed. The patient returned to care approximately two years later due to a painful nodule in the right lower leg. A skin biopsy showed metastatic EHE from the lung. We used a safety margin of 1 cm based on clinical experience, because no prior case had been reported regarding the resection margin appropriate for primary cutaneous EHE and skin metastases of PEH. At four months after surgery, the patient recovered without complications or recurrence. Skin metastasis of PEH is extremely rare, and only two cases have been reported in the literature. In this case, we report a rare case of PEH with histologically diagnosed skin metastasis that was successfully treated by curative resection. It is expected that this case report will provide a helpful contribution to the extant data regarding PEH metastases.