1.Current diagnosis and treatment of skull base osteomyelitis.
Journal of Clinical Otorhinolaryngology Head and Neck Surgery 2023;37(7):588-592
Skull base osteomyelitis is a rare, refractory, and potentially fatal disease primarily caused by otogenic and sino rhinogenic infections. At times, it can mimic neoplasia complicating the diagnosis. With the use of antibiotics, advancements in diagnostic methods, and skull base surgical techniques, the mortality rate has significantly improved. However, the successful diagnosis and treatment of the disease is still challenging due to delayed diagnosis, lengthy treatment course, a tendency for relapse and lack of guidelines. Therefore, this article aims to review the progress in the diagnosis and treatment of skull base osteomyelitis.
Humans
;
Otitis Externa/diagnosis*
;
Skull Base
;
Osteomyelitis/complications*
;
Anti-Bacterial Agents/therapeutic use*
;
Diagnosis, Differential
2.Arthroscopic Treatment for Septic Arthritis of the Shoulders in Neonates: A Case Report.
Kyoung Jin PARK ; Hyung Ki LEE
Clinics in Shoulder and Elbow 2016;19(3):163-167
Septic arthritis in neonates is a rare condition. A failure to make an early diagnosis of septic arthritis in neonates may leave a permanent disability as a result of a delayed treatment. Thus, septic arthritis, requires a prompt diagnosis and a timely treatment especially in this subset of patients. In this case report, we describe our treatment protocol for septic arthritis and concurrent osteomyelitis in the right shoulder of a 28-day-old newborn. Using 2.4 mm wrist arthroscopy, we performed an arthroscopic irrigation and drainage, to remove intra-articular debris and inflammatory tissue, and multiple drilling. We report a satisfactory clinical outcome without any postoperative complications or side effects.
Arthritis, Infectious*
;
Arthroscopy
;
Clinical Protocols
;
Diagnosis
;
Drainage
;
Early Diagnosis
;
Humans
;
Infant, Newborn*
;
Osteomyelitis
;
Postoperative Complications
;
Shoulder Joint
;
Shoulder*
;
Wrist
3.Arthroscopic Treatment for Septic Arthritis of the Shoulders in Neonates: A Case Report
Kyoung Jin PARK ; Hyung Ki LEE
Journal of the Korean Shoulder and Elbow Society 2016;19(3):163-167
Septic arthritis in neonates is a rare condition. A failure to make an early diagnosis of septic arthritis in neonates may leave a permanent disability as a result of a delayed treatment. Thus, septic arthritis, requires a prompt diagnosis and a timely treatment especially in this subset of patients. In this case report, we describe our treatment protocol for septic arthritis and concurrent osteomyelitis in the right shoulder of a 28-day-old newborn. Using 2.4 mm wrist arthroscopy, we performed an arthroscopic irrigation and drainage, to remove intra-articular debris and inflammatory tissue, and multiple drilling. We report a satisfactory clinical outcome without any postoperative complications or side effects.
Arthritis, Infectious
;
Arthroscopy
;
Clinical Protocols
;
Diagnosis
;
Drainage
;
Early Diagnosis
;
Humans
;
Infant, Newborn
;
Osteomyelitis
;
Postoperative Complications
;
Shoulder Joint
;
Shoulder
;
Wrist
4.Avoiding diagnostic pitfalls in mimics of neoplasia: the importance of a comprehensive diagnostic approach.
Ely Zarina SAMSUDIN ; Tunku KAMARUL ; Azura MANSOR
Singapore medical journal 2015;56(5):e92-5
Any medical diagnosis should take a multimodal approach, especially those involving tumour-like conditions, as entities that mimic neoplasms have overlapping features and may present detrimental outcomes if they are underdiagnosed. These case reports present diagnostic pitfalls resulting from overdependence on a single diagnostic parameter for three musculoskeletal neoplasm mimics: brown tumour (BT) that was mistaken for giant cell tumour (GCT), methicillin-resistant Staphylococcus aureus osteomyelitis mistaken for osteosarcoma and a pseudoaneurysm mistaken for a soft tissue sarcoma. Literature reviews revealed five reports of BT simulating GCT, four reports of osteomyelitis mimicking osteosarcoma and five reports of a pseudoaneurysm imitating a soft tissue sarcoma. Our findings highlight the therapeutic dilemmas that arise with musculoskeletal mimics, as well as the importance of thorough investigation to distinguish mimickers from true neoplasms.
Adult
;
Aneurysm, False
;
diagnosis
;
Biopsy
;
Bone Diseases
;
diagnosis
;
Bone Diseases, Metabolic
;
diagnosis
;
Bone Neoplasms
;
diagnosis
;
Cell Proliferation
;
Diagnosis, Differential
;
Diagnostic Errors
;
prevention & control
;
Female
;
Giant Cell Tumors
;
diagnosis
;
Humans
;
Hyperparathyroidism
;
complications
;
Leukocytosis
;
diagnosis
;
Male
;
Methicillin-Resistant Staphylococcus aureus
;
Middle Aged
;
Neoplasms
;
diagnosis
;
microbiology
;
Osteomyelitis
;
diagnosis
;
microbiology
;
Osteosarcoma
;
diagnosis
;
Sarcoma
;
diagnosis
;
Soft Tissue Neoplasms
;
diagnosis
;
Tibia
;
pathology
5.Magnetic resonance imaging of diabetic foot complications.
Keynes T A LOW ; Wilfred C G PEH
Singapore medical journal 2015;56(1):23-quiz 34
This pictorial review aims to illustrate the various manifestations of the diabetic foot on magnetic resonance (MR) imaging. The utility of MR imaging and its imaging features in the diagnosis of pedal osteomyelitis are illustrated. There is often difficulty encountered in distinguishing osteomyelitis from neuroarthropathy, both clinically and on imaging. By providing an accurate diagnosis based on imaging, the radiologist plays a significant role in the management of patients with complications of diabetic foot.
Aged
;
Aged, 80 and over
;
Cellulitis
;
diagnosis
;
Diabetic Foot
;
complications
;
diagnosis
;
Female
;
Gangrene
;
diagnosis
;
Humans
;
Inflammation
;
Magnetic Resonance Imaging
;
Male
;
Middle Aged
;
Osteomyelitis
;
diagnosis
;
physiopathology
;
Risk Factors
;
Skin Diseases
;
diagnosis
;
Ulcer
;
diagnosis
6.A case of peripheral gangrene and osteomyelitis secondary to terlipressin therapy in advanced liver disease.
Clinical and Molecular Hepatology 2013;19(2):179-184
Variceal bleeding and hepatorenal syndrome (HRS) are serious and life-threatening complications of advanced liver disease. Terlipressin is widely used to manage both acute variceal bleeding and HRS due to its potency and long duration of action. The most severe (though rare) adverse event is ischemia. The present report describes the case of a patient with gangrene and osteomyelitis secondary to terlipressin therapy. A 71-year-old male with alcoholic liver cirrhosis (Child-Pugh B) and chronic hepatitis C was admitted due to a drowsy mental status. The patient had several experiences of orthopedic surgery. His creatinine level had gradually elevated to 4.02 mg/dL, and his urine output decreased to 500 mL/24 hr. The patient was diagnosed as having grade III hepatic encephalopathy (HE) and type II HRS. Terlipressin and albumin were administered intravenously to treat the HRS over 11 days. Although he recovered from the HE and HRS, the patient developed peripheral gangrene and osteomyelitis in both feet. His right toes were cured with the aid of rescue therapy, but his left three toes had to be amputated. Peripheral gangrene and osteomyelitis secondary to terlipressin therapy occur only rarely, and there is no specific rescue therapy for these conditions. Thus, attention should be paid to the possibility of ischemia of the skin and bone during or after terlipressin therapy.
Aged
;
Creatinine/blood
;
Foot/pathology
;
Gangrene/*etiology
;
Hepatitis C, Chronic/complications
;
Humans
;
Liver Cirrhosis/complications/diagnosis
;
Liver Diseases/*diagnosis/drug therapy
;
Lypressin/adverse effects/*analogs & derivatives/therapeutic use
;
Male
;
Osteomyelitis/*etiology
;
Severity of Illness Index
;
Toe Phalanges/radiography
;
Vasoconstrictor Agents/*adverse effects/therapeutic use
7.A Case of IgM Deficiency with B Cell Deficiency Detected by ABO Discrepancy in a Patient with Acute Osteomyelitis.
Chae Lim JUNG ; Mi Kyung CHA ; Byoung Hyuk JUN ; Ki Sook HONG
Annals of Laboratory Medicine 2013;33(3):208-211
ABO discrepancy refers to an inconsistency between red cell and serum typings and has various causes, including hypogammaglobulinemia. IgM deficiency is a rare disorder that may accompany several conditions such as infection and autoimmune disorders. Here, we describe a case of IgM deficiency discovered during the evaluation of an ABO discrepancy in a 16-yr-old Korean boy. ABO blood grouping showed that while his cell type was O+, serum typing detected only anti-A (3+). Anti-B was not detectable at room temperature but was graded at 1+ at 4degrees C. ABO genotyping revealed an O/O genotype. His serum IgG, IgA, and IgM concentrations were 770 mg/dL (reference range: 800-1,700 mg/dL), 244 mg/dL (reference range: 100-490 mg/dL), and 13.5 mg/dL (reference range: 50-320 mg/dL), respectively. He was diagnosed with acute osteomyelitis on the basis of clinical presentation and imaging studies. The symptoms gradually improved within 3 weeks of treatment. However, the ABO discrepancy and IgM deficiency persisted even 6 months after recovery and lymphocyte subset analysis revealed CD19+ B cell deficiency. To the best of our knowledge, IgM deficiency detected by ABO discrepancy in a patient with acute osteomyelitis has not been reported before.
ABO Blood-Group System/genetics
;
Acute Disease
;
Adolescent
;
B-Lymphocytes/cytology/immunology/metabolism
;
Bone and Bones/radionuclide imaging
;
Genotype
;
Humans
;
Immunoglobulin A/blood
;
Immunoglobulin G/blood
;
Immunoglobulin M/blood
;
Immunologic Deficiency Syndromes/complications/*diagnosis
;
Knee/radionuclide imaging
;
Magnetic Resonance Imaging
;
Male
;
Osteomyelitis/complications/*diagnosis
;
Radiopharmaceuticals/diagnostic use
8.A Case of IgM Deficiency with B Cell Deficiency Detected by ABO Discrepancy in a Patient with Acute Osteomyelitis.
Chae Lim JUNG ; Mi Kyung CHA ; Byoung Hyuk JUN ; Ki Sook HONG
Annals of Laboratory Medicine 2013;33(3):208-211
ABO discrepancy refers to an inconsistency between red cell and serum typings and has various causes, including hypogammaglobulinemia. IgM deficiency is a rare disorder that may accompany several conditions such as infection and autoimmune disorders. Here, we describe a case of IgM deficiency discovered during the evaluation of an ABO discrepancy in a 16-yr-old Korean boy. ABO blood grouping showed that while his cell type was O+, serum typing detected only anti-A (3+). Anti-B was not detectable at room temperature but was graded at 1+ at 4degrees C. ABO genotyping revealed an O/O genotype. His serum IgG, IgA, and IgM concentrations were 770 mg/dL (reference range: 800-1,700 mg/dL), 244 mg/dL (reference range: 100-490 mg/dL), and 13.5 mg/dL (reference range: 50-320 mg/dL), respectively. He was diagnosed with acute osteomyelitis on the basis of clinical presentation and imaging studies. The symptoms gradually improved within 3 weeks of treatment. However, the ABO discrepancy and IgM deficiency persisted even 6 months after recovery and lymphocyte subset analysis revealed CD19+ B cell deficiency. To the best of our knowledge, IgM deficiency detected by ABO discrepancy in a patient with acute osteomyelitis has not been reported before.
ABO Blood-Group System/genetics
;
Acute Disease
;
Adolescent
;
B-Lymphocytes/cytology/immunology/metabolism
;
Bone and Bones/radionuclide imaging
;
Genotype
;
Humans
;
Immunoglobulin A/blood
;
Immunoglobulin G/blood
;
Immunoglobulin M/blood
;
Immunologic Deficiency Syndromes/complications/*diagnosis
;
Knee/radionuclide imaging
;
Magnetic Resonance Imaging
;
Male
;
Osteomyelitis/complications/*diagnosis
;
Radiopharmaceuticals/diagnostic use
9.Bilateral Brodie's abscess at the proximal tibia.
Halil BULDU ; Fikri Erkal BILEN ; Levent ERALP ; Mehmet KOCAOGLU
Singapore medical journal 2012;53(8):e159-60
Brodie's abscess is a form of subacute osteomyelitis, which typically involves the metaphyses of the long tubular bones, particularly in the tibia. The diagnosis is usually made incidentally, as there are no accompanying symptoms or laboratory studies. Bilateral involvement at the proximal tibia is unusual. However, orthopaedic surgeons should be aware of this entity, as it may present without symptoms. Checking the contralateral limb for concomitant Brodie's abscess is recommended.
Abscess
;
diagnosis
;
Adult
;
Female
;
Humans
;
Osteomyelitis
;
complications
;
diagnosis
;
Radiography
;
Tibia
;
diagnostic imaging
;
pathology
10.A Case of Atypical Skull Base Osteomyelitis with Septic Pulmonary Embolism.
Soon Jung LEE ; Young Cheol WEON ; Hee Jeong CHA ; Sun Young KIM ; Kwang Won SEO ; Yangjin JEGAL ; Jong Joon AHN ; Seung Won RA
Journal of Korean Medical Science 2011;26(7):962-965
Skull base osteomyelitis (SBO) is difficult to diagnose when a patient presents with multiple cranial nerve palsies but no obvious infectious focus. There is no report about SBO with septic pulmonary embolism. A 51-yr-old man presented to our hospital with headache, hoarseness, dysphagia, frequent choking, fever, cough, and sputum production. He was diagnosed of having masked mastoiditis complicated by SBO with multiple cranial nerve palsies, sigmoid sinus thrombosis, and septic pulmonary embolism. We successfully treated him with antibiotics and anticoagulants alone, with no surgical intervention. His neurologic deficits were completely recovered. Decrease of pulmonary nodules and thrombus in the sinus was evident on the follow-up imaging one month later. In selected cases of intracranial complications of SBO and septic pulmonary embolism, secondary to mastoiditis with early response to antibiotic therapy, conservative treatment may be considered and surgical intervention may be withheld.
Anti-Bacterial Agents/therapeutic use
;
Anticoagulants/therapeutic use
;
C-Reactive Protein/analysis
;
Cranial Nerve Diseases/complications/diagnosis
;
Diagnosis, Differential
;
Enterobacter aerogenes/isolation & purification
;
Enterobacteriaceae Infections/diagnosis/drug therapy
;
Humans
;
Lung/pathology/radiography
;
Magnetic Resonance Imaging
;
Male
;
Mastoiditis/complications/diagnosis
;
Middle Aged
;
Osteomyelitis/complications/*diagnosis/drug therapy
;
Pulmonary Embolism/complications/*diagnosis/microbiology
;
Sinus Thrombosis, Intracranial/complications/diagnosis
;
Skull Base
;
Sputum/microbiology
;
Tomography, X-Ray Computed

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