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1.
J Cardiovasc Med (Hagerstown) ; 25(7): 529-538, 2024 Jul 01.
Article in English | MEDLINE | ID: mdl-38829939

ABSTRACT

AIMS: This study assessed the outcomes of concomitant mitral valve disease and severe aortic stenosis in patients undergoing transcatheter aortic valve replacement (TAVR). METHODS: Echocardiographic data of 813 patients with severe aortic stenosis undergoing transfemoral TAVR were collected, and clinical outcomes were analyzed for individuals with mitral stenosis and mitral regurgitation. RESULTS: The final cohort includes 788 patients with severe calcific aortic stenosis. Among single parameters of mitral stenosis, a smaller baseline mitral valve area (MVA) by the continuity equation and higher postprocedural mean mitral gradients (MMG) were associated with an increased risk of death at 1 year (P-values 0.02 and <0.01, respectively), but no correlation with outcomes was demonstrated after multivariate adjustment for major prognosticators. Mitral stenosis (based on MVA + MMG) was not associated with complications or mortality. Mitral regurgitation was present in 94.6% of the population at baseline and regressed by at least one grade post-TAVR in 28% of the patients. The improvement in mitral regurgitation was associated with a greater prosthetic effective orifice area (P-value 0.03). Significant (at least moderate) residual mitral regurgitation was correlated with short-term complications and shown to be an independent predictor of 1-year mortality (P-value 0.02, odds ratio (OR) 5.37, confidence interval 1.34-21.5). CONCLUSION: Mitral regurgitation has a greater impact on TAVR patients than mitral stenosis as assessed by functional methods.


Subject(s)
Aortic Valve Stenosis , Mitral Valve Insufficiency , Mitral Valve Stenosis , Transcatheter Aortic Valve Replacement , Humans , Male , Female , Mitral Valve Stenosis/surgery , Mitral Valve Stenosis/diagnostic imaging , Mitral Valve Stenosis/mortality , Mitral Valve Stenosis/physiopathology , Mitral Valve Stenosis/complications , Mitral Valve Insufficiency/surgery , Mitral Valve Insufficiency/physiopathology , Mitral Valve Insufficiency/mortality , Mitral Valve Insufficiency/diagnostic imaging , Mitral Valve Insufficiency/complications , Transcatheter Aortic Valve Replacement/adverse effects , Transcatheter Aortic Valve Replacement/mortality , Aged, 80 and over , Aortic Valve Stenosis/surgery , Aortic Valve Stenosis/mortality , Aortic Valve Stenosis/diagnostic imaging , Aortic Valve Stenosis/physiopathology , Aortic Valve Stenosis/complications , Aged , Treatment Outcome , Severity of Illness Index , Retrospective Studies , Prognosis , Risk Factors , Aortic Valve/surgery , Aortic Valve/diagnostic imaging , Aortic Valve/physiopathology , Aortic Valve/pathology , Calcinosis/mortality , Calcinosis/diagnostic imaging , Calcinosis/complications , Mitral Valve/diagnostic imaging , Mitral Valve/surgery , Mitral Valve/physiopathology , Echocardiography
2.
Tex Heart Inst J ; 51(1)2024 May 07.
Article in English | MEDLINE | ID: mdl-38711341

ABSTRACT

A 62-year-old woman who had undergone mitral valve replacement 24 years ago was admitted to the hospital with congestive heart failure. She needed heart transplantation for stage D heart failure. Preoperative cardiac computed tomographic scans showed a severely calcified left atrium and a large right atrium. Given that the left atrium's calcification was too severe to suture, the calcified left atrial wall was broadly resected, and the resected left atrial wall was reconstructed with a bovine pericardial patch for anastomosis with the donor's left atrial wall. The operation was completed without heavy bleeding, and the patient was discharged from the hospital with no complications.


Subject(s)
Calcinosis , Heart Atria , Heart Failure , Heart Transplantation , Rheumatic Heart Disease , Tomography, X-Ray Computed , Humans , Female , Rheumatic Heart Disease/surgery , Rheumatic Heart Disease/complications , Rheumatic Heart Disease/diagnosis , Heart Transplantation/methods , Middle Aged , Calcinosis/surgery , Calcinosis/diagnosis , Calcinosis/complications , Heart Atria/diagnostic imaging , Heart Atria/surgery , Heart Failure/surgery , Heart Failure/etiology , Heart Failure/diagnosis , Severity of Illness Index , Treatment Outcome , Heart Valve Prosthesis Implantation/methods , Pericardium/transplantation , Pericardium/surgery
3.
Clin Respir J ; 18(5): e13773, 2024 May.
Article in English | MEDLINE | ID: mdl-38725329

ABSTRACT

BACKGROUND: Pulmonary alveolar microlithiasis (PAM) is a rare autosomal recessive genetic disorder with approximately 1000 known cases worldwide, in which calcium phosphate microliths deposit in the alveolar air spaces. As of writing this report, no definitive conventional therapy exists, and many PAM cases may progress to severe respiratory failure and potential death. Bilateral lung transplantation (BLx) seems to be the most optimal solution; however, this procedure is challenging along with limited reports regarding the outcome in PAM. We report a case of PAM successfully treated with BLx for the first time in Iran. METHOD: We present the case of a 42-year-old female with a longstanding history of cough, not responding to conventional antitussive medication, who was diagnosed as a case of PAM following a hospitalization due to coughing, dyspnea on exertion, and hemoptysis. Despite treatment with corticosteroid and medical treatment, no improvement was achieved and she subsequently developed respiratory and right ventricular failure, with oxygen ventilation dependence. Eventually, she was scheduled for BLx. The operation was successful and during her 2-year follow-up, no recurrence or significant postoperative complications has been reported. CONCLUSION: This case presentation and literature review confirm the effectiveness of BLx as a promising treatment for PAM-diagnosed patients, improving both life expectancy and quality of life.


Subject(s)
Calcinosis , Lung Diseases , Lung Transplantation , Humans , Female , Lung Transplantation/methods , Adult , Lung Diseases/surgery , Lung Diseases/complications , Calcinosis/surgery , Calcinosis/complications , Calcinosis/diagnosis , Treatment Outcome , Genetic Diseases, Inborn/surgery , Genetic Diseases, Inborn/complications , Genetic Diseases, Inborn/diagnosis , Tomography, X-Ray Computed/methods , Cough/etiology , Iran , Quality of Life
4.
Neurocase ; 30(1): 48-53, 2024 02.
Article in English | MEDLINE | ID: mdl-38757414

ABSTRACT

Fahr's disease is a rare neurodegenerative disorder with brain calcifications and neuropsychiatric symptoms. It can have variable phenotypic expression and intermittent symptomatology, making diagnosis challenging. In this report, we describe a young female patient presenting with symptoms of psychosis and confusion, which could be indicative of a delirium superimposed on the cerebral vulnerability associated with Fahr's disease. Notably, about two years prior, she experienced multiple episodes of tonic-clonic seizures that spontaneously resolved without pharmacological intervention. She had no previous psychiatric history. Following comprehensive investigations, other organic causes were ruled out, and Fahr's disease was diagnosed based on bilateral symmetrical brain calcifications seen on a head CT scan. Her treatment regimen encompassed antipsychotics and anticonvulsants. This case highlights the importance of considering Fahr's disease as a differential diagnosis in patients with new-onset neuropsychiatric symptoms. The case also explores the atypical early onset and intermittent nature of symptoms in the absence of a positive family history, highlighting the complexity of Fahr's disease. A multidisciplinary approach and regular follow-up are crucial for optimizing patient care and monitoring disease progression. Further research is needed to enhance our understanding of Fahr's disease and develop standardized treatment strategies for this rare condition.


Subject(s)
Calcinosis , Neurodegenerative Diseases , Humans , Female , Calcinosis/complications , Calcinosis/diagnosis , Neurodegenerative Diseases/diagnosis , Neurodegenerative Diseases/complications , Psychotic Disorders/etiology , Psychotic Disorders/diagnosis , Adult , Basal Ganglia Diseases/diagnosis , Basal Ganglia Diseases/physiopathology , Basal Ganglia Diseases/complications , Confusion/etiology , Confusion/diagnosis
5.
Endocr Regul ; 58(1): 101-104, 2024 Jan 01.
Article in English | MEDLINE | ID: mdl-38656253

ABSTRACT

Diabetes mellitus type 3 refers to diabetes secondary to an existing disease or condition of the exocrine pancreas and is an uncommon cause of diabetes occurring due to pancreatogenic pathology. It accounts for 15-20% of diabetic patients in Indian and Southeast Asian continents. This is case report of a rare case of type 3 diabetes mellitus (T3DM) presenting with diabetic ketoacidosis (DKA). The patient was admitted for DKA along with complaint of hyperglycemia, blood glucose of 405 mg/dl with HbA1c level of 13.7%. Computed tomography evidence revealed chronic calcific pancreatitis with intraductal calculi and dilated pancreatic duct.


Subject(s)
Calcinosis , Calculi , Diabetic Ketoacidosis , Pancreatic Ducts , Pancreatitis, Chronic , Humans , Diabetic Ketoacidosis/complications , Diabetic Ketoacidosis/diagnosis , Pancreatitis, Chronic/complications , Pancreatitis, Chronic/diagnosis , Pancreatitis, Chronic/diagnostic imaging , Calculi/complications , Calculi/diagnostic imaging , Calculi/diagnosis , Pancreatic Ducts/pathology , Pancreatic Ducts/diagnostic imaging , Calcinosis/etiology , Calcinosis/diagnosis , Calcinosis/complications , Calcinosis/diagnostic imaging , Male , Adult , Tomography, X-Ray Computed
6.
Medicina (Kaunas) ; 60(4)2024 Apr 04.
Article in English | MEDLINE | ID: mdl-38674241

ABSTRACT

Soft tissue calcifications frequently appear on imaging studies, representing a prevalent but non-specific discovery, varying from a local reaction without clear cause to suggesting an underlying systemic condition. Because calcifications like these can arise from various causes, an accurate differential diagnosis is crucial. Differential diagnosis entails a methodical assessment of the patient, encompassing clinical presentation, medical history, radiological and pathological findings, and other pertinent factors. Through scrutiny of the patient's medical and trauma history, we can refine potential causes of calcification to vascular, metabolic, autoimmune, neoplastic, or traumatic origins. Furthermore, routine laboratory assessments, including serum levels of calcium, phosphorus, ionized calcium, vitamin D metabolites, and parathyroid hormone (PTH), aid in identifying metabolic etiologies. We describe a rare occurrence of osteoma cutis in a 15-year-old female patient with a history of pseudohypoparathyroidism (PHP) and Albright's hereditary osteodystrophy (AHO). The patient presented with a painful mass on the lateral side of her left foot. The diagnosis was based on medical history, laboratory tests, and imaging, leading to an excisional biopsy and complete pain relief post-surgery. Understanding such rare occurrences and related conditions is crucial for accurate diagnosis and management.


Subject(s)
Calcinosis , Pseudohypoparathyroidism , Humans , Female , Calcinosis/complications , Calcinosis/diagnostic imaging , Pseudohypoparathyroidism/complications , Pseudohypoparathyroidism/diagnosis , Adolescent , Diagnosis, Differential , Foot , Bone Diseases, Metabolic/complications , Bone Diseases, Metabolic/diagnosis
7.
J Cardiothorac Surg ; 19(1): 143, 2024 Mar 19.
Article in English | MEDLINE | ID: mdl-38504317

ABSTRACT

BACKGROUND: Coronary artery obstruction after percutaneous aortic replacement is a complication with high short-term mortality secondary to the lack of timely treatment. There are various predictors of coronary obstruction prior to valve placement such as the distance from the ostia, the degree of calcification, the distance from the sinuses; In such a situation some measures must be taken to prevent and treat coronary obstruction. CASE PRESENTATION: An 84-year-old male, with severe aortic stenosis and high surgical risk, who was treated with TAVR. However, during the deployment of the valve he presented hemodynamic instability secondary to LMCA obstruction. The intravascular image showed obstruction of the ostium secondary to the displacement of calcium that he was successfully treated with a chimney stent technique. CONCLUSIONS: The high degree of calcification and the left ostium near the annulus are conditions for obstruction of the ostium at the time of valve release; In this context, provisional stenting prior to TAVR in patients at high risk of obstruction should be considered as a safe prevention strategy to achieve the success of the procedure.


Subject(s)
Aortic Valve Stenosis , Calcinosis , Coronary Occlusion , Heart Valve Prosthesis , Transcatheter Aortic Valve Replacement , Male , Humans , Aged, 80 and over , Transcatheter Aortic Valve Replacement/adverse effects , Transcatheter Aortic Valve Replacement/methods , Aortic Valve/surgery , Coronary Vessels/surgery , Heart Valve Prosthesis/adverse effects , Risk Factors , Treatment Outcome , Coronary Occlusion/etiology , Calcinosis/complications , Calcinosis/surgery , Aortic Valve Stenosis/complications , Prosthesis Design
8.
Leg Med (Tokyo) ; 68: 102431, 2024 May.
Article in English | MEDLINE | ID: mdl-38460208

ABSTRACT

Mitral annular calcification (MAC) is a chronic and degenerative condition involving calcification of the mitral annulus. MAC is a risk factor for coronary artery disease, cardiovascular events, stroke, and cardiovascular death. However, patients with MAC are often asymptomatic. Herein, we present the first case of cardiac tamponade due to infection of MAC in forensic pathology. An 80-year-old woman was found in cardiopulmonary arrest shortly after experiencing fatigue. She was transferred to a hospital, and despite chest compression and ventilation, she was pronounced dead due to no response. Postmortem computed tomography, autopsy, and histological examination showed MAC, abscess formation involving Gram-positive cocci on the MAC, and fistulation of the abscess into the intracardial pericardial cavities, resulting in a massive lethal hemopericardium.


Subject(s)
Autopsy , Calcinosis , Mitral Valve , Pericardial Effusion , Humans , Female , Aged, 80 and over , Calcinosis/pathology , Calcinosis/complications , Mitral Valve/pathology , Pericardial Effusion/pathology , Fatal Outcome , Cardiac Tamponade/etiology , Heart Valve Diseases/pathology , Heart Valve Diseases/complications , Forensic Pathology/methods , Abscess/pathology , Abscess/complications , Heart Arrest/etiology
9.
J Med Case Rep ; 18(1): 98, 2024 Mar 10.
Article in English | MEDLINE | ID: mdl-38461261

ABSTRACT

BACKGROUND: Familial calcific band-shaped keratopathy (BSK) is a very rare disease, with no underlying cause. There is no underlying disease in this form of the disease. This article introduces a family with seven children, three of whom were diagnosed with familial primary calcific BSK. One of them developed a systemic disease 38 years after ocular manifestation. CASE PRESENTATION: In this case report, three Iranian siblings from a family with familial calcific band-shaped keratopathy (BSK) are introduced. Systemic and ocular examinations performed on these patients indicated the occurrence of chronic kidney disease in the older child, a 41-year-old woman, 38 years after ocular manifestation. The examinations conducted on the other two siblings revealed no pathological findings. The 41-year-old sister and 37-year-old brother underwent unilateral deep anterior lamellar keratoplasty (DALK), while the 33-year-old sister underwent bilateral superficial keratectomy (SK). CONCLUSION: Considering the late onset of systemic disease in one of the siblings diagnosed with familial calcific band-shaped keratopathy (BSK), it is crucial to emphasize the necessity of long-term follow-up for these patients and their families.


Subject(s)
Calcinosis , Corneal Dystrophies, Hereditary , Male , Child , Female , Humans , Adolescent , Adult , Iran , Corneal Dystrophies, Hereditary/surgery , Eye/pathology , Calcinosis/complications , Calcinosis/diagnostic imaging , Calcinosis/genetics , Retrospective Studies
10.
Article in English | MEDLINE | ID: mdl-38320892

ABSTRACT

OBJECTIVE: The aim was to optimize diagnostics for carotid artery calcifications (CACs) on panoramic radiographs (PRs) to identify cardiovascular disease (CVD) by investigating how 4 defined CAC shapes are associated with ultrasound (US) findings indicating CVD. STUDY DESIGN: The study included 414 participants (802 neck sides) from the Malmö Offspring Dental Study, examined with PRs. The PRs were assessed for CAC shapes stratified into 4 categories: single, scattered, vessel-width defining, and vessel-outlining. The carotid arteries were examined with US for signs of CVD: the presence of plaques, largest individual area of a plaque, number of plaques, and percentage reduction of the lumen. Associations between the different CAC categories and US characteristics were analyzed. RESULTS: All categories of CAC were significantly associated with a higher degree of US findings indicating CVD compared with no CAC (P < .001). The most significant differences were found for vessel-outlining CAC, with the mean of the largest individual plaque area of 17.9 vs 2.3 mm2, mean number of plaques 1.6 vs 0.2, and mean percentage reduction of the lumen 24.1% vs 3.5% (all P < .001). CONCLUSIONS: Independent of shape, CACs detected on PRs were associated with a higher degree of US findings of CVD. This was most pronounced for vessel-outlining CAC. With refined differential diagnostics of CACs in PRs, dentists may contribute to improved identification of patients in need of cardiovascular prevention.


Subject(s)
Calcinosis , Cardiovascular Diseases , Carotid Artery Diseases , Plaque, Atherosclerotic , Humans , Cardiovascular Diseases/diagnostic imaging , Cardiovascular Diseases/complications , Radiography, Panoramic , Carotid Artery Diseases/diagnostic imaging , Carotid Artery Diseases/complications , Plaque, Atherosclerotic/complications , Carotid Arteries/diagnostic imaging , Calcinosis/diagnostic imaging , Calcinosis/complications , Risk Factors
12.
Eur J Prev Cardiol ; 31(6): 732-741, 2024 Apr 18.
Article in English | MEDLINE | ID: mdl-38300625

ABSTRACT

AIMS: Lipoprotein(a) [Lp(a)] is an atherogenic lipid particle associated with increased risk for coronary heart disease (CHD) events. Coronary artery calcium (CAC) score is a tool to diagnose subclinical atherosclerosis and guide clinical decision-making for primary prevention of CHD. Studies show conflicting results concerning the relationship between Lp(a) and CAC in asymptomatic populations. We conducted a meta-analysis to evaluate the association of Lp(a) and CAC in asymptomatic patients. METHODS AND RESULTS: We systematically searched PubMed, Embase, and Cochrane until April 2023 for studies evaluating the association between Lp(a) and CAC in asymptomatic patients. We evaluated CAC > 0 Agatston units, and CAC ≥ 100. Lp(a) was analysed as a continuous or dichotomous variable. We assessed the association between Lp(a) and CAC with pooled odds ratios (OR) adopting a random-effects model. A total of 23 105 patients from 18 studies were included in the meta-analysis with a mean age of 55.9 years, 46.4% female. Elevated Lp(a) increased the odds of CAC > 0 [OR 1.31; 95% confidence intervals (CI) 1.05-1.64; P = 0.02], CAC ≥100 (OR 1.29; 95% CI 1.01-1.65; P = 0.04; ), and CAC progression (OR 1.43; 95% CI 1.20-1.70; P < 0.01; ). For each increment of 1 mg/dL in Lp(a) there was a 1% in the odds of CAC > 0 (OR 1.01; 95% CI 1.01-1.01; P < 0.01). CONCLUSION: Our findings of this meta-analysis suggest that Lp(a) is positively associated with a higher likelihood of CAC. Higher Lp(a) levels increased the odds of CAC >0. These data support the concept that Lp(a) is atherogenic, although with high heterogeneity and a low level of certainty. PROTOCOL REGISTRATION: CRD42023422034. KEY FINDINGS: Asymptomatic patients with elevated Lp(a) had 31% higher chances of having any coronary calcification (CAC > 0) and 29% higher chances of having more advanced calcification (CAC > 100). It increased the chances of having progression of coronary calcification over time by 43%. For each 1 mg/dL of Lp(a) there was an increment of 1% chance of having coronary calcification.


We conducted a meta-analysis to evaluate the association between Lp(a) and coronary calcification in asymptomatic patients without a known history of coronary artery disease.


Subject(s)
Atherosclerosis , Calcinosis , Coronary Artery Disease , Vascular Calcification , Humans , Female , Middle Aged , Male , Calcium , Coronary Artery Disease/complications , Risk Factors , Coronary Vessels , Lipoprotein(a) , Atherosclerosis/complications , Calcinosis/complications
13.
BMC Musculoskelet Disord ; 25(1): 118, 2024 Feb 09.
Article in English | MEDLINE | ID: mdl-38336663

ABSTRACT

BACKGROUND: Intervertebral disc calcification (IDC) combined with calcification in children has been sporadically reported, while ossification of the posterior longitudinal ligament (OPLL) in the cervical spine in pediatric patients is exceedingly rare. The aim of this study is to investigate the potential prognosis and outcomes associated with this condition. CASE PRESENTATION: We present an unusual case involving a 10-year-old Chinese child diagnosed with calcified cervical disc herniation and ossification of the posterior longitudinal ligament. Conservative treatment measures were implemented, and at the 1-month and 6-month follow-up, the patient's pain exhibited significant improvement. Subsequent cervical MRI and CT scans revealed the complete disappearance of OPLL and substantial absorption of the calcified disc. During the three-month follow-up, CT demonstrated slight residual disc calcification, however, the patient remained asymptomatic with no discernible limitation in cervical motion. CONCLUSIONS: We conducted a comprehensive review of several cases presenting with the same diagnosis. It is noteworthy that IDC combined with OPLL in children constitutes a rare clinical entity. Despite imaging indications of potential spinal canal occupation, the majority of such cases demonstrate complete absorption following conservative treatment, with OPLL exhibiting a faster absorption rate than calcified discs.


Subject(s)
Calcinosis , Chondrocalcinosis , Intervertebral Disc Degeneration , Intervertebral Disc , Ossification of Posterior Longitudinal Ligament , Humans , Child , Longitudinal Ligaments/diagnostic imaging , Osteogenesis , Intervertebral Disc Degeneration/complications , Intervertebral Disc Degeneration/diagnostic imaging , Ossification of Posterior Longitudinal Ligament/complications , Ossification of Posterior Longitudinal Ligament/diagnostic imaging , Ossification of Posterior Longitudinal Ligament/therapy , Calcinosis/complications , Calcinosis/diagnostic imaging , Calcinosis/therapy , Chondrocalcinosis/complications , Cervical Vertebrae/diagnostic imaging , Intervertebral Disc/diagnostic imaging
14.
J Med Case Rep ; 18(1): 58, 2024 Feb 17.
Article in English | MEDLINE | ID: mdl-38365754

ABSTRACT

BACKGROUND: Bursitis is the inflammation of a synovial bursa, a small synovial fluid-filled sac that acts as a cushion between muscles, tendons, and bones. Further, calcific bursitis results from calcium deposits on the synovial joint that exacerbates pain and swelling. The Gruberi bursa is located dorsolaterally in the ankle, between the extensor digitorium longus and the talus. Despite limited literature on its pathophysiology, the aim of this case is to discuss the bursa's association with calcific bursitis and its management via a case presented to our clinic. CASE PRESENTATION: A 47-year-old Caucasian female with no past medical or family history presents with acute right ankle pain following a minor injury 3 months prior with no improvement on analgesic or steroid therapy. Imaging demonstrated incidental calcium deposits. The day prior to presentation, the patient stated she used 1-pound ankle weights that resulted in mild swelling and gradual pain to the right dorsoanterior ankle. Physical exam findings displayed a significant reduction in the range of motion limited by pain. Imaging confirmed calcification within the capsule of the talonavicular joint, consistent with Gruberi bursitis. Initial management with prednisone yielded minimal improvement, requiring an interventional approach with ultrasound-guided barbotage that elicited immediate improvement. CONCLUSION: The presented case report highlights a rare and unique instance of acute ankle pain and swelling caused by calcific Gruberi bursitis in a young female. Although the Gruberi bursa is a relatively new discovery, it contains inflammatory components that may predispose it to calcification and should be considered in the differential of ankle swelling. Therefore, utilizing a systematic approach to a clinical presentation and considering all differential diagnoses is essential.


Subject(s)
Bursitis , Calcinosis , Humans , Female , Middle Aged , Bursa, Synovial/diagnostic imaging , Calcium , Bursitis/diagnostic imaging , Ultrasonography/methods , Arthralgia/etiology , Calcinosis/diagnostic imaging , Calcinosis/complications
16.
Pain Manag ; 14(1): 29-33, 2024 Jan.
Article in English | MEDLINE | ID: mdl-38189140

ABSTRACT

Calcification of the medial collateral ligament is a rare cause of medial knee pain along with functional impairment. Most cases are asymptomatic but those that are symptomatic typically respond to conservative management. However, in those instances with persistent symptoms that desire further intervention but want to minimize the risks associated with surgery, we present a novel approach for calcium removal with an ultrasound-guided percutaneous needle tenotomy with TenJet™ as a reasonable treatment modality.


Subject(s)
Calcinosis , Medial Collateral Ligament, Knee , Humans , Medial Collateral Ligament, Knee/diagnostic imaging , Medial Collateral Ligament, Knee/surgery , Knee Joint/diagnostic imaging , Knee Joint/surgery , Calcinosis/complications , Calcinosis/diagnostic imaging , Calcinosis/surgery , Ultrasonography , Ultrasonography, Interventional
17.
J Wound Care ; 33(1): 66-71, 2024 Jan 02.
Article in English | MEDLINE | ID: mdl-38197282

ABSTRACT

Foot ulceration and infection is associated with a substantial increase in morbidity and mortality in patients with diabetes. We present a clinical case of recurrent diabetic foot infection with an atypical clinical evolution. A 58-year-old male patient with type 1 diabetes and a history of bilateral Charcot foot neuroarthropathy was followed at our Diabetic Foot Clinic for an unhealed plantar foot ulcer for >1.5 years with recurrent episodes of infection. He was admitted to hospital due to foot ulcer reinfection with sepsis and ipsilateral lower limb cellulitis. The foot infection was found to be associated with an underlying abscess in the anterior compartment of the leg, with a cutaneous fistulous course with extensive alterations of an inflammatory nature. Exudate from the lesion was drained and tissue biopsied, revealing Serratia marcescens and Klebsiella oxytoca with dystrophic calcification (DC). Surgical excision of dystrophic tissue with debridement of the fistulous tracts was performed. The excised material corroborated the presence of fibroadipose connective tissue with marked DC, as well as areas of mixed inflammation compatible with a chronic infectious aetiology. Targeted long-term antibiotic therapy was implemented, for a total of six weeks, with a favourable clinical evolution and complete closure of the lesion at the final follow-up. DC results from calcium deposition in degenerated tissues without evidence of systemic mineral imbalance and is a potential cause of non-healing ulcers. Few cases of DC have been reported in diabetic foot patients and its treatment remains challenging and controversial. A longer follow-up period is necessary to verify the effectiveness of our approach.


Subject(s)
Calcinosis , Diabetes Mellitus , Diabetic Foot , Sepsis , Skin Diseases , Male , Humans , Middle Aged , Diabetic Foot/complications , Leg , Abscess , Calcinosis/complications
19.
Australas J Dermatol ; 65(2): 171-173, 2024 Mar.
Article in English | MEDLINE | ID: mdl-38066726

ABSTRACT

Calcinosis cutis is represented by the deposition of insoluble calcium salts in the skin and subcutaneous tissue. Calcinosis can lead to repeated episodes of local inflammation and repeated infections, resulting in pain and functional disability, and even death. Here, we present a case of a patient with SSc who experienced calcinosis universalis and eventually died from recurrent infections at the sacrococcygeal calcification.


Subject(s)
Calcinosis , Scleroderma, Systemic , Skin Diseases , Humans , Skin Diseases/complications , Scleroderma, Systemic/complications , Calcinosis/complications , Skin , Subcutaneous Tissue
20.
Physiother Res Int ; 29(1): e2042, 2024 Jan.
Article in English | MEDLINE | ID: mdl-37493215

ABSTRACT

BACKGROUND: Tendinopathy is caused by repetitive motion, excessive stress on the tendon, overstretch, and motion past the critical angle of rotation or translation. There are various treatment options available for tendinitis, including those affecting both the upper and lower limbs and those of calcific and non-calcific types. HYPOTHESIS/PURPOSE: Few reviews have analyzed the efficacy of Extracorporeal Shockwave Therapy (ESWT) in treating upper and lower limb tendinopathies while considering calcific and non-calcific-type tendinitis. This paper provides a review and meta-analysis on Randomized Controlled Trials (RCTs), which compared results from a group undergoing ESWT treatment to another group under different treatments. STUDY DESIGN: Systematic review and meta-analysis. METHODS: A systematic search was conducted on PubMed, Web of Science, Embase, the Cochrane Central Register of Control Trials (CENTRAL), and Physiotherapy Evidence Database (PEDro) databases for articles published up to January 2022. The reference lists of identified articles were further scanned. Twenty-two studies were included in the meta-analysis. RESULTS: Meta-analysis showed no difference in pain reduction in ESWT when compared with a comparison group at 4 (p = 0.26) and 12 weeks (p = 0.33). There were no differences in DASH scores at 12 months between the two groups (p = 0.32). CONCLUSION: Extracorporeal Shockwave Therapy (ESWT) is effective when used to treat lower limb and calcific tendinitis. It does not yield any better results than other treatment options in managing upper limb tendinopathies and non-calcific tendinopathies.


Subject(s)
Calcinosis , Tendinopathy , Humans , Calcinosis/complications , Calcinosis/therapy , Extracorporeal Shockwave Therapy/adverse effects , Extracorporeal Shockwave Therapy/methods , High-Energy Shock Waves/therapeutic use , Lower Extremity , Shoulder Pain/therapy , Tendinopathy/therapy , Treatment Outcome
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