• 제목/요약/키워드: misdiagnosis

검색결과 199건 처리시간 0.023초

Successful Treatment of Rectus Femoris Calcification with Ultrasound-guided Injection: A Case Report

  • Hong, Myong Joo;Kim, Yeon Dong;Park, Jeong Ki;Kang, Tai Ug
    • The Korean Journal of Pain
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    • 제28권1호
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    • pp.52-56
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    • 2015
  • Painful periarticular calcification most commonly occurs within the rotator cuff of the shoulder and rarely around the elbow, hip, foot, and neck. As acute inflammatory reaction develops, severe pain, exquisite tenderness, local swelling, and limitation of motion with pain occur. In case of calcific tendinitis of the shoulder, it can be easily diagnosed according to the symptoms and with x-ray. However, in lesions of the hip, as it is a rare location and usually involves pain in the posterolateral aspect of the thigh, which can simulate radicular pain from a lumbar intervertebral disc, it could be difficult to diagnose. Hence, physicians usually focus on lumbar lesions; therefore, misdiagnosis is common and leads to a delayed management. Here, we report the case of a 30-year-old female patient with calcific tendinitis of the rectus femoris that was successfully managed with ultrasound-guided steroid injection. This study offers knowledge about the rectus femoris calcification.

성문에서 발생한 재발성 흉선상 방추상 상피세포 종양(Spindle Epithelial Tumor with Thymus-Like Differentiation, SETTLE) 1예 (A Case of Recurrent Spindle Cell Epithelial Tumor of Thymus-Like Differentiation (SETTLE) in the Glottis)

  • 박우리;최나연;정만기
    • 대한후두음성언어의학회지
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    • 제26권2호
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    • pp.133-136
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    • 2015
  • Spindle epithelial tumor with thymus-like differentiation (SETTLE) is an extremely rare type of thyroid tumor, with spares reports on its clinical course. SETTLE is derived from branchial pouch or thymic remnants, and classified as a low grade, malignant neoplasm due to its indolent growth and tendency to develop delayed metastasis. Therefore, stringent initial workups and long-term follow-up are required to prevent misdiagnosis. We present a case of recurrent spindle epithelial tumor with thymus-like differentiation (SETTLE) in the glottis of 57 year-old male patient, who had a history of surgical excision for the SETTLE from the thyroid gland 5 years ago. Transoral CO2 laser surgery was performed to remove the glottic tumor and there was no evidence of local recurrence at 11 months postoperatively.

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소아 대퇴탈장의 중요성 (The Importance of Femoral Hernia in Children)

  • 한석주;최봉수;한애리;오정탁;최승훈;황의호
    • Advances in pediatric surgery
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    • 제6권2호
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    • pp.124-127
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    • 2000
  • Femoral hernia is very rare in children and is easily misdiagnosed. During a period of three years, three children with femoral hernia were treated by one pediatric surgeon at Severance Hospital. Only one case was diagnosed correctly before surgery, and the others were thought to be either an indirect inguinal hernia or groin mass. Curative hernioplasty (McVay hernioplasty) could be done in only one case at the time of first operation. Diagnosis of femoral hernia in children is a challenge because of rarity and similarity of clinical presentation to indirect inguinal hernia. Co-incidental findings of indirect inguinal hernia sac or patent processus vaginalis during surgery can perpetuate the misdiagnosis. In case of absence of expected indirect inguinal hernia or apparent recurrence of indirect inguinal hernia, one should consider the possibility of femoral hernia.

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하악과두에 발생된 골연골증 (OSTEOCHONDROMA OF THE MANDIBULAR CONDYLE)

  • 정기훈;김은경
    • 치과방사선
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    • 제23권2호
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    • pp.373-378
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    • 1993
  • 저자들은 희귀한 하악과두의 골연골종으로 진단 내려진 27세 남성 환자에서 아래와 같은 사항을 관찰하였다. 1. 임상적으로 좌측안면부의 비대칭과, 교합이상 그리고 저작 시 좌측 악관절의 동통이 있었다. 2. 방사선학적으로 좌측과두에 내측으로 균일한 방사선불투과성의 종괴가 보였으며, 좌측 하악지 길이의 증가 및 우측으로의 하악 변위가 관찰되었다. 또 골스캔상에서 좌측 악관절부위의 hot spot이 관찰되었다. 3. 조직병리학적으로 불규칙한 골의 형성과 연골모를 볼 수 있었다.

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Primary intraosseous squamous cell carcinoma mimicking periapical disease: a case report

  • Choi, Yoon-Joo;Oh, Song-Hee;Kang, Ju-Han;Choi, Hwa-Young;Kim, Gyu-Tae;Yu, Jae-Jung;Choi, Yong-Suk;Hwang, Eui-Hwan
    • Imaging Science in Dentistry
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    • 제42권4호
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    • pp.265-270
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    • 2012
  • Primary intraosseous squamous cell carcinoma (PIOSCC) is a rare carcinoma, which arises within the jaws without connection to the oral mucosa and presumably develops from a remnant of odontogenic epithelium. We present a case of solid type PIOSCC in a 52-year-old male patient complaining of dull pain on his left lower molar. In this case, early stage PIOSCC mimicking a periapical lesion might lead to a one-year delay in treatment due to the misdiagnosis of osteomyelitis after extraction of the third molar. The clinical, radiological, and histologic features are described. In this case, there was initial radiographic evidence for PIOSCC mimicking a periapical lesion. Incautious radiographic interpretation and treatment procedures had delayed the correct diagnosis and resulted in extensive bony destruction during the patient's disease progression.

지속적인 고열을 동반한 폐렴양 결핵병변 1예 (A Case of Tuberculous Pneumonitis With Continuous High Spiking Fever)

  • 차봉수;김세규;이홍열;장준;김성규;이원영
    • Tuberculosis and Respiratory Diseases
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    • 제41권3호
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    • pp.302-306
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    • 1994
  • A 33-year old male was admitted due to continuous high spiking fever for 2 months via local clinic. He had been diagnosed pulmonary tuberculosis at local clinic. However, spiking fever had not been controlled by anti-tuberculous medications. Chest PA showed confluent consolidation on right upper & mid-lung field. 5 anti-tuberculous regimens(Streptomycin, Isoniazid, Rifampin, Ethambutol, Pyrazinamaide) were administered initially and steroid therapy was followed for relieving toxic symptoms Very slowly resolved chest X-ray lesion and continuous fever suggested the possibility of misdiagnosis. After 60th hospital day, the chest X-ray lesion was resolved gradually and fever subsided almost completely. He was discharged on 76th hospital day with anti-tuberculous drugs and steroid(prednisolon), without any other problems except sustained mild fever.

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A Case of Yellow Nail Syndrome: Misdiagnosis as Congestive Heart Failure

  • Bae, Byeong-Joo;Kim, Hee-Joung;Kim, Sun-Jong;Lee, Kye-Young;Kim, Won-Dong;Yoo, Kwang-Ha
    • Tuberculosis and Respiratory Diseases
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    • 제71권1호
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    • pp.46-49
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    • 2011
  • Yellow nail syndrome (YNS) is a rare disorder of unknown cause associated with yellow nails, lymphedema and respiratory manifestations. It was first described by Samman and White in 1964, and to date, approximately 150 cases have been reported. The diagnosis of YNS is essentially a clinical one and based on the presence of characteristic findings. We report a case of YNS of a 62-year-old female who presented with a 4-month history of dyspnea and recurrent pleural effusion. The patient had a 5-year history of leg swelling and dyspnea. She had been managed with medications for congestive heart failure (CHF) for two years and she was referred to our hospital for further evaluation and management.

다발성 백반증을 동반한 태선양 이형성증 (LICHENOID DYSPLASIA ASSOCIATED WITH MULTIPLE LEUKOPLAKIA : A CASE REPORT)

  • 안신영;문철웅;윤정훈;김수관
    • Maxillofacial Plastic and Reconstructive Surgery
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    • 제27권6호
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    • pp.565-569
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    • 2005
  • Lichenoid dysplasia is a lesion similar to oral lichen planus with epithelial dysplasia. It can be clinically mistaken for oral lichen planus, but has histologic features of dysplasia and a true malignant predisposition. It is not a variant or transitional form of lichen planus but, instead, represents a distinct entity that has a true potential for malignant transformation. In addition to abnormal epithelial maturation and cytology, lichenoid dysplasia exhibits other histologic features that separate it from oral lichen planus. Lichenoid dysplasia and lichen planus share many clinical and microscopic features, leading to the frequent misdiagnosis of unrecognized lichenoid dysplasia as lichen planus. We experienced a case of lichenoid dysplasia in the oral mucosa. We treated this patient with surgical excision. The patient has now been followed for two months. It is important to recognize this precancerous condition and inspect the excision site and remaining oral mucosa during long-term follow-up.

Case Report of the Squamous Cell Carcinoma in a Patient with Oral Lichen Planus

  • Woo, Keoncheol;Oh, Duwon;Kwon, Jeong-Seung;Ahn, Hyung-Joon;Choi, Jong-hoon
    • Journal of Oral Medicine and Pain
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    • 제41권2호
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    • pp.72-75
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    • 2016
  • Lichen planus is a chronic disease characterized by bilateral and multiple lesions on the skin or oral mucosa. Lichen planus is caused by immune mediated degeneration along the border between epithelium and connective tissue. The incidence of oral squamous cell carcinoma in patients diagnosed with oral lichen planus (OLP) is reported to be between 0.4%-5.6% in different studies and the World Health Organization has categorized lichen planus as "a potentially malignant disorder". However, the correlation between OLP and oral cancer still remains controversial as some reported that the reason for increased incidence of squamous cell carcinoma in OLP patient is misdiagnosis of dysplastic lesion as OLP. This report aims to discuss the correlation between OLP and oral cancer through a case of middle aged woman diagnosed with OLP who was successfully treated but developed squamous cell carcinoma 8 years later.

구강건조증과 구취 : 최신 지견의 고찰 (Xerostomia and halitosis : A review and current concepts)

  • 이연희
    • 대한치과의사협회지
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    • 제55권9호
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    • pp.640-656
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    • 2017
  • Xerostomia is usually caused by a reduced salivary flow or by changes in the biochemical composition of saliva. Halitosis or oral malodor is an offensive odor usually originating from the oral cavity. Halitosis can lead to anxiety and psychosocial embarrassment. The occurrence of halitosis closely related with intraoral conditions including the presence of xerostomia. Especially, the relationship between xerostomia and halitosis is prominent in elderly patients receiving polypharmacy with at least two systemic diseases. This study is a review of the update literature of xerostomia and halitosis. A large number of papers have been searched and identified using the words , , , , , , and . Papers not relevant to the issue were removed reducing the entries to 79 only. Most of identified papers were systematic reviews, non-systematic reviews, and observational studies. With a proper diagnosis, identification of the etiology and timely referrals certain steps are taken to create a successful individualized therapeutic approach. It is significant to highlight the necessity of an interdisciplinary method for the treatment of xerostomia and halitosis to prevent misdiagnosis or unnecessary treatment. This article concisely focuses on the development of a systemic flow of events to come to the proper treatment of the xerostomia and halitosis.

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