Aggressive Chondroblastoma Report of a Case with Multiple Bone and Soft Tissue Involvement

1977 ◽  
Vol &NA; (126) ◽  
pp. 261???265 ◽  
Author(s):  
MEREDITH T. HULL ◽  
F. GONZALEZ-RUSSI ◽  
G. PAUL DEROSA ◽  
RICHARD S. GRAUL
2019 ◽  
Vol 27 (3) ◽  
pp. 230949901988121 ◽  
Author(s):  
Hasan U Oğur ◽  
Rana Kapukaya ◽  
Özgür Külahçı ◽  
Cengiz Yılmaz ◽  
Kemal Yüce ◽  
...  

Aim: To investigate the diagnosis and treatment methods of soft tissue involvement of hydatid cysts (HCs). Materials and Methods: Eleven patients who were diagnosed as having HC with muscular tissue (soft tissue) involvement between 2010 and 2016 were evaluated retrospectively. Seven patients had typical HC magnetic resonance imaging (MRI) and four patients had cysts with an unusual appearance. We evaluated how to diagnose the cysts using imaging methods, their characteristic radiologic images, and treatment alternatives against the disease. The patients were treated with antihelminthic chemotherapy preoperatively and postoperatively. Results: Of the 11 patients who underwent treatment, 7 were diagnosed using MRI and 4 were diagnosed with histopathologic examinations. The mean follow-up period was 16 (range, 6–24) months, and the mean age was 39.4 (range, 24–56) years. In seven patients, multivesicular appearance with specific MRI findings, T2-hypointense rim appearance, double-rim sign, membrane dissociation, and appearance of daughter cysts were identified as diagnostic criteria. Two patients underwent ultrasound assisted percutaneous aspiration–injection–reaspiration (PAIR) treatment. Seven patients underwent total pericystectomy, and two patients underwent subtotal pericystectomy with serum saline injection into the cyst. Two patients showed signs of mild anaphylaxis, one during the diagnosis and one during treatment. Conclusion: There may be difficulties in the diagnosis and treatment of HCs of the musculoskeletal system. It should be known that there are alternative methods in the treatment (cyst excision and PAIR treatment). Clinical, serologic, and radiologic findings should be used in the diagnosis. To avoid complications during the histopathologic diagnosis, MRI should be examined in detail. It is thought that atypical cysts can be diagnosed (double-layer appearance and peripheral rim sign) in addition to typical cysts (detached membrane and multivesicular appearance), and diagnosis and treatment can be planned without anaphylactic complications.


Blood ◽  
2007 ◽  
Vol 110 (11) ◽  
pp. 3557-3557
Author(s):  
Michela Rondoni ◽  
Stefania Paolini ◽  
Ernesto Vigna ◽  
Serena Merante ◽  
Michele Malagola ◽  
...  

Abstract Idiopathic hypereosinophilic syndrome (HES) is a rare hematological disorder characterized by persistent eosinophilia presenting often with organ involvement. The increased blood and tissue levels of eosinophils (eos) appear to produce tissue damage via local release of toxic substances producing inflammation and fibrosis. Data from the literature are fragmentary and deduced from several historical series. The most commonly involved organs reported are cardiovascular, pulmonary, cutaneous and neurologic systems. Cardiac disease is described as the major cause of morbidity and mortality. Due to the new knowledge about myeloproliferative variant of HES and PDGFRA rearrangement, we tried to identify different clinical picture. The aim of this retrospective analysis is to evaluate the prevalence of HES-related organ damage, its relation to F/P status, and response to imatinib therapy. A prospective multicenter study of the HES began in 2001. Patient enrolled had HES diagnosis, independently of presence of FIP1L1-PDGFRA (F/P) rearrangement. 72 patients were treated with IM 100 to 400 mg daily with a median observation time of 28 months (r 12–68). 33 patients (46%) were positive for the F/P rearrangement (F/P+), while 39 (54%) were negative (F/P−). At the time of enrolment HES patients were systematically screened for organ damage with instrumental evaluation (chest radiography, echocardiogram, abdomen ultrasonography). Symptoms were considered too, so if respiratory symptoms were presented or a reduction of ejection fraction was found organ involvement was established. Results. Organ involvement was recorded in 42% of F/P+ and in 51% of F/P−. Skin involvement was only recorded in F/P−, whereas splenomegaly was reported in 7 F/P+ and only in one case of F/P−. To date, soft tissue was peculiar site of F/P+ patients. All the 33 F/P+ patients achieved a complete hematologic remission (CHR) and molecular negativity, and together they became negative for organ localization and free of symptoms. In the two patients with soft tissue involvement (temporal/parietal and retro-orbital masses) imaging response was documented with positron emission tomography (PET) and with CT scan one month after the beginning of the therapy. Favourable response was recorded also in patients with cardiac involvement, apiece to grade of fibrosis. 5 out of 39 F/P− patients achieved a transitory CHR, but no durable effects on organ involvement. All these patients are alive. Conclusion. Organ involvement do not seems to be a constant characteristic of HES, irrespective to F/P status, but there are differences between F/P+ and F/P− patients. Organ damage in F/P+ subset is reversible before fibrosis development. In the whole population observed, no deaths were recorded in more than five years. F/P+(33 pt) F/P−(39 pt) Statistic Organ damage 42% 51% p=NS More than 1 organ involvement 18% 3% p=0,01 Heart 15% 5% p=NS Lung 18% 26% p=NS Spleen 21% 3% 0,001 Skin 0 15% p=0,001 Liver 3% 3% p=NS Soft tissue 6% 0 p=0,1 Skeleton 3% 0 p=NS Gut 0 3% p=NS


2011 ◽  
Vol 21 (4) ◽  
pp. 465-467 ◽  
Author(s):  
Funda Öztunç ◽  
Bülent Koca ◽  
İbrahim Adaletli

AbstractGeneralised lymphangiomatosis is a rare disease that is characterized by widespread bony and soft tissue involvement of lymphangioma. Radiological evaluation is crucial because the site and extent of the lymphangioma are important prognostic factors. The computed tomography, ultrasonography and magnetic resonance images showed sharply defined, non-enhanced cystic lesions involving the mediastinum, bones, spleen, lung, and lower neck. We report here a case that was referred to us for investigation of marked cardiomegaly.


1997 ◽  
Vol 22 (7) ◽  
pp. 508 ◽  
Author(s):  
ZSUZSANNA BORDY ◽  
ERZSÉBET PASZTARAK ◽  
GYÖRGY BÁNSÁGI ◽  
ERZSÉBET SIK

2018 ◽  
Vol 43 (11) ◽  
pp. 854-856
Author(s):  
Derya Çayir ◽  
Mehmet Bozkurt ◽  
Salih Sinan Gültekin ◽  
Alper Özgür Karaçalioğlu

2019 ◽  
Vol 11 (1) ◽  
pp. 21-25 ◽  
Author(s):  
Ricardo J. Dinis-Oliveira

Background: Coma blisters or coma bullae are bullous lesions that have been associated with cases of drug overdose-induced coma. Previous history of suicide attempt by administering benzodiazepines, barbiturates, ethanol, antipsychotics, antidepressants or opioids have been particularly implicated. Patients may present also painful deep skin and soft tissue involvement, edema and functional impairment. The pathophysiology remains unknown and lesions are usually self-limited and typically resolve without scarring. Objective: This work aims to fully review the state of the art regarding the causes pathophysiology, diagnosis and treatment of drug overdose-induced coma blisters. Conclusion: Coma blisters are a benign, self-limiting condition that should be suspected in patients who develop pressure blisters several hours after an altered state of consciousness.


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