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Nepal Med Coll J ; — May 11, Qualitative and quantitative dermatoglyphic traits in patients with breast cancer: a prospective clinical study. BMC Cancer ; Dermatoglyphics: a predictor tool to analyze the occurrence of breast cancer. A cross-sectional study on the palmar dermatoglyphics in relation to carcinoma breast patients. J Clin Diagn Res ; — Digital dermatoglyphics and breast cancer. Breast Cancer Res Treat ; — Dermatoglyphic study in breast carcinoma patients. Int J Sci Res ; — Study of dermatoglyphic patterns of hands in women with breast cancer.

Pak J Med Sci ; — Hawthorne M. Fingerprint pattern types and associated terminology. In: Fingerprints analysis and understanding. Fingerprint patterns, a novel risk factor for breast cancer in Egyptian populations: a case—control study.

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Egypt J Surg ; Figure 1 Ridge Count from core to delta point Hawthorne, [21]. Click here to view. Figure 2 Whorl pattern. Figure 3 Radial loop pattern. Figure 4 Ulnar loop pattern. Figure 5 Arch pattern. Table 1 Fingerprint pattern in right hand Click here to view. Table 2 Fingerprint pattern in Lt hand Click here to view.

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Table 3 Ridge count in right hand Click here to view. Table 4 Mean and standard deviation of right hand Click here to view. Table 5 Ridge count in left hand Click here to view. Table 6 Mean and standard deviation of left hand Click here to view. Table 7 Counting whorl pattern in all fingers of diseased and control groups Click here to view. Table 8 Frequency of whorls between diseased and control group Click here to view. Related articles breast cancer fingerprint finger ridge count. Access Statistics. One-third of ECD patients have xanthelasma, occurring as yellow eyelid plaques, as in our case.

Other sites of xanthogranulomatous involvement are the face, neck, axilla, trunk, and groin, and may appear as yellow or red-brown papules that merge into plaques. It is impossible to distinguish between xanthogranulomatous lesion of ECD and adult juvenile xanthogranulomatous JXG disease on the basis of skin lesions alone, but unlike ECD, JXG is less commonly a multi-system disease [ 10 ]. The typical diffuse skeletal involvement with symmetric sclerosis of the long bones is a distinct pattern of bone involvement of Erdheim-Chester disease [ 25 ]. Therefore, we evaluated skeletal involvement in our patient.

Plain radiography of both tibias showed mild diffuse osteosclerotic changes. In some patients with ECD, plain films may be not conclusive; therefore, technetiumm bone scintigraphy, which can explore the whole skeleton, is mandatory and very valuable in this situation. The axial skeleton is usually spared in cases of ECD but iliac bone involvement has been reported before [ 18 ], as in our patient. This was confirmed by the bone marrow biopsy taken from iliac bone, which revealed hypocellular marrow with infiltration by fatty cells histocytes.

Thus, bone scintigraphy may be beneficial for early detection of skeletal involvement of ECD [ 26 ] and this role is more important in the case of un-obvious changes in plain radiography, as shown in this patient. Retroperitoneal involvement is described in more than one-third of patients with ECD and is often asymptomatic. This finding, due to the perirenal fat infiltration, appears as an irregular renal border that is emphasized by iodinated contrast and is useful for differential diagnosis with idiopathic or secondary retroperitoneal fibrosis [ 6 ].

Because of the rarity of the condition and the paucity of clinical trials, there is no definite treatment for ECD. Indeed, we have now treated our patient with systemic steroids and azathioprine for 2 months with good stabilization and no recurrence of pleural and pericardial effusion and slight improvement of visual acuity in the left eye. Although the clinical symptoms of our patient seem to be stable, there have been few reports of the efficacy of these regimens [ 27 , 28 ]. Therefore, close long-term follow-up will be required to evaluate the efficacy of these treatments in our patient, and searching for another effective therapy is mandatory.

A promising dual therapy with anakinra, an interleukinreceptor antagonist, and vemurafenib, the BRAF V kinase inhibitor, was associated with a sustained abatement in symptoms for months [ 29 ]. We presented the case of an ECD patient with multi-organ involvement, diagnosed after the passage of more than 6 years from the onset of disease. This report emphasizes the need for a high index of suspicion in this diagnosis.

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We hope to be able to perform long-term follow-up to accurately evaluate treatment efficacy and prognosis. This study was not conducted with research intervention, so Ethics Committee approval was not necessary. The authors have no funding or conflicts of interest to disclose. Read article at publisher's site DOI : Case Rep Oncol , 10 2 , 01 May Onco Targets Ther , , 24 Jan To arrive at the top five similar articles we use a word-weighted algorithm to compare words from the Title and Abstract of each citation.

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J Fr Ophtalmol , 37 5 , 24 Mar Cited by: 0 articles PMID: Medicine Madr , 94 43 :e, 01 Oct Klin Monbl Augenheilkd , 11 , 01 Nov Cited by: 2 articles PMID: Dtsch Med Wochenschr , 39 , 20 Sep Diagn Cytopathol , 42 6 , 28 Feb Coronavirus: Find the latest articles and preprints. Europe PMC requires Javascript to function effectively.

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Search articles by 'Emad E Abdellateef'. Abdellateef EE 1 ,. Search articles by 'Ayman R Abdelhai'. Abdelhai AR 1 ,.

Search articles by 'Heba H Gawish'. Gawish HH 2 ,. Search articles by 'Ghada A Abdulmonaem'. Abdulmonaem GA 3 ,. Search articles by 'Eman H Abdelbary'. Abdelbary EH 4 ,. Search articles by 'Ahmed I Ahmed'. Ahmed AI 1. Affiliations 3 authors 1. Share this article Share with email Share with twitter Share with linkedin Share with facebook. Our patient's young age and stable clinical status may allow long-term follow-up of treatment results.

Free full text. Am J Case Rep. Published online May PMID: Emad E. Abdelbary , D, 4 and Ahmed I. Ahmed B, 1. Ayman R. Heba H. Ghada A. Eman H. Ahmed I. Author information Article notes Copyright and License information Disclaimer. Corresponding Author: Ayman R. Abdelhai, e-mail: ku. Received Jan 8; Accepted Mar This article has been cited by other articles in PMC. Go to:. Background: Erdheim-Chester disease is a rare non-Langerhans-cell histiocytosis of unknown etiology with multi-organ involvement.

Case Report: A year-old woman presented with orthopnea, severe fatigue, bilateral exophthalmos, and gradual loss of vision. Conclusions: This report describes the first case presentation of Erdheim-Chester disease in our country. Open in a separate window. Figure 1. Table 1. The laboratory results of our patient during the period of her hospital admission.

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Table 2. Currently, Dr. Al Hawamidiyah. The SEM image Figures 1 a and 1 b revealed changes in surface morphology of raw material as it underwent both physical and chemical carbonization. Obesity and pregnancy: A transversal study from a low-risk maternity.

Radiological and imaging findings Chest radiography showed cardiomegaly and an urgent echocardiography showed a large pericardial effusion with echocardiographic features of cardiac tamponade. Figure 2. Figure 3. Figure 4. Figure 5. Figure 6.