Displaying publications 101 - 120 of 5116 in total

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  1. Majid ZA, Siar CH, Ling KC
    Med J Malaysia, 1986 Jun;41(2):179-82.
    PMID: 3821617
    An unusual case of fibrous epulis in a newborn is presented. The clinical appearance, histological features and method of treatment are described. A short review of the literature is also included.
    Matched MeSH terms: Alveolar Process/pathology*; Connective Tissue/pathology; Fibroblasts/pathology; Fibromatosis, Gingival/pathology*
  2. Muhsein KA, Liew NC, Shaker AR, Shahrin IA
    Asian J Surg, 2004 Jan;27(1):54-7.
    PMID: 14719517
    Castleman's disease is a rare lymphoproliferative disorder of unknown aetiology. The presentation is varied, diagnosis is difficult, and optimum management is still unknown. We report our experience with a case of Castleman's disease in a 34-year old woman who presented with pallor, hepatosplenomegaly, and a right iliac fossa mass that was 5 cm in diameter. this was initially diagnosed as a soft tissue sarcoma and preoperative tumour embolization was planned before excision. Mesenteric arteriogram revealed that the feeder arteries arose from the superior mesenteric artery and embolization was aborted for fear of causing bowel ischaemia. On laparotomy, lymphoid enlargement was found between the leaves of the jejunal mesentery. The tumour was relatively avascular and the overlying mesenteric vessels contributed to teh duplex ultrasound and computerized tomography appearance of hypervascularity. The tumour with the mesentery and the overlying segment of jejunum was excised completely. Histopathology confirmed Castleman's disease. The purpose of this report is to present this rare case that caused a diagnostic dilemma and to review the management of this disorder.
    Matched MeSH terms: Giant Lymph Node Hyperplasia/pathology*; Ilium/pathology*; Jejunum/pathology; Peritoneal Diseases/pathology*
  3. Mayya A, Eachempati P, Nagraj SK, Kumar K
    BMJ Case Rep, 2020 Jun 09;13(6).
    PMID: 32522723 DOI: 10.1136/bcr-2020-234297
    Matched MeSH terms: Hemangioma/pathology*; Maxilla/pathology; Mouth, Edentulous/pathology*; Palate/pathology*
  4. Mohd Fuad SK, Adznan N, Hayati AR, Virasamy V, Rahim NS
    Malays J Pathol, 2020 Dec;42(3):439-444.
    PMID: 33361726
    INTRODUCTION: Chronic histiocytic intervillositis (CHI) is a rare placental lesion strongly associated with recurrent miscarriages and fetal losses. It requires histopathological diagnosis and can only be made after delivery of the products of conception (POC). We describe a case of CHI in a 41-yearold lady with a 16-year history of thirteen recurrent consecutive first trimester miscarriages.

    CASE REPORT: The patient is a 41-year-old lady who suffered first trimester miscarriages in all her thirteen pregnancies. The relevant clinical investigations revealed neither significant nor helpful findings in determining the cause of recurrent miscarriages. Histological findings in each except one of the submitted conceptual tissue showed similar features of histiocytic aggregates primarily within the intervillous spaces, a characteristic description of CHI. One of the samples showed degenerative changes.

    DISCUSSION: Practicing pathologists are not familiar with the histological features of CHI and this may be a potential pitfall in routine examination of POCs. Recognising this entity allows for accurate diagnosis and hence better management. The aetiology remains unclear, although an immunopathological basis are being explored.

    Matched MeSH terms: Abortion, Habitual/pathology*; Placenta Diseases/pathology*; Histiocytosis/pathology; Aborted Fetus/pathology*
  5. Subramanyam C, Lal M
    Med J Malaya, 1970 Jun;24(4):306-7.
    PMID: 4248354
    Matched MeSH terms: Choriocarcinoma/pathology*; Nasopharyngeal Neoplasms/pathology*; Nose Neoplasms/pathology*; Uterine Neoplasms/pathology
  6. Sinniah D, Nagappan N, Choo M
    Med J Malaysia, 1979 Dec;34(2):164-6.
    PMID: 548721
    Matched MeSH terms: Fingers/pathology*; Lymph Nodes/pathology*; Lymphatic Diseases/pathology*; Mucocutaneous Lymph Node Syndrome/pathology*
  7. Loke YW
    Br. J. Cancer, 1965 Sep;19(3):482-5.
    PMID: 5833066 DOI: 10.1038/bjc.1965.56
    Matched MeSH terms: Adenocarcinoma/pathology; Carcinoma, Squamous Cell/pathology*; Lymph Nodes/pathology*; Nasopharyngeal Neoplasms/pathology*
  8. Raymond AA, Isa MR, Abdullah T, Kudva MV
    Singapore Med J, 1993 Jun;34(3):276-8.
    PMID: 8266193
    A 41-year-old Malay housewife presented with recurrent chylous ascites and progressive cachexia over 17 years. A diagnosis of lymphangioleiomyomatosis (LAM) was established by laparotomy where biopsy of the liver, peritoneum and adhesions from previous surgery showed smooth muscle proliferation in the blood vessels and lymphatics. Clinically and radiologically, there was no evidence of pulmonary involvement. She was treated with dietary fat restriction and medium-chain triglycerides. This is the first case of LAM reported in Malaysia.
    Matched MeSH terms: Chylous Ascites/pathology*; Liver Neoplasms/pathology*; Peritoneal Neoplasms/pathology*; Lymphangioleiomyomatosis/pathology*
  9. Müller S, Boy SC, Day TA, Magliocca KR, Richardson MS, Sloan P, et al.
    Arch Pathol Lab Med, 2019 04;143(4):439-446.
    PMID: 30500296 DOI: 10.5858/arpa.2018-0411-SA
    The International Collaboration on Cancer Reporting is a nonprofit organization whose goal is to develop evidence-based, internationally agreed-upon standardized data sets for each cancer site for use throughout the world. Providing global standardization of pathology tumor classification, staging, and other reporting elements will lead to the objective of improved patient management and enhanced epidemiologic research. Carcinomas of the oral cavity continue to represent a significant oncologic management burden, especially as changes in alcohol and tobacco use on a global scale contribute to tumor development. Separation of oral cavity carcinomas from oropharyngeal tumors is also important, as management and outcome are quite different when human papillomavirus association is taken into consideration. Topics such as tumor thickness versus depth of invasion, pattern of invasive front, extent and size of perineural invasion, and margin assessment all contribute to accurate classification and staging of tumors. This review focuses on the data set developed for Carcinomas of the Oral Cavity Histopathology Reporting Guide, with discussion of the key elements developed for inclusion.
    Matched MeSH terms: Carcinoma/pathology*; Mouth Neoplasms/pathology*; Pathology, Clinical/standards
  10. Ebin LE, Zam NM, Othman SA
    Aust Orthod J, 2010 Nov;26(2):165-70.
    PMID: 21175027
    To investigate the craniofacial morphology of Malay children with repaired UCLP and compare the data with non-cleft Malay children.
    Matched MeSH terms: Chin/pathology; Cleft Lip/pathology*; Cleft Palate/pathology*; Incisor/pathology; Lip/pathology; Mandible/pathology; Maxilla/pathology; Nose/pathology; Skull Base/pathology
  11. Dayapala A, Kumar V
    Am J Forensic Med Pathol, 2009 Jun;30(2):171-4.
    PMID: 19465810 DOI: 10.1097/PAF.0b013e3181875a79
    Sudden deaths because of congenital heart diseases are infrequently referred to the forensic pathologist for autopsy. Many of such deaths, if already diagnosed are released directly from the hospital without autopsy. Even forensic pathologists face a few difficulties in performing the autopsy on such infrequent cases, as they are not always updated with the anatomy of anomalies. While dealing with such cases, the concerned forensic pathologist is compelled to refer literature and textbooks again to understand the nature of developmental defects. This is especially so when dealing with cases of situs inversus accompanied by transposition of great arteries and other congenital cardiac abnormalities and variants such as single ventricle, double outlet right ventricle, Taussig-Bing variety etc. In the present case also, situs inversus with transposition of great vessels and other anomalies have been noted and studied.
    Matched MeSH terms: Coronary Vessel Anomalies/pathology; Cyanosis/pathology; Heart Defects, Congenital/pathology*; Heart Ventricles/pathology; Mitral Valve Stenosis/pathology; Myocardium/pathology*; Pulmonary Artery/pathology; Situs Inversus/pathology*; Forensic Pathology
  12. Hasnan J, Jayaram G
    Malays J Pathol, 1996 Jun;18(1):35-41.
    PMID: 10879223
    Fine needle aspiration (FNA) cytology is now an integral part of the pre-operative investigation of breast lesions and the therapeutic protocol is today often planned on the basis of cytodiagnosis. However, from time to time the cytological picture may be equivocal or inconclusive. In recent years, nucleolar organizer region (NOR) scores have been explored for potential value in the diagnosis of malignancy as the scores in malignant nuclei are seen to be higher than in benign or reactive nuclei. With a view to applying NOR scoring in the evaluation of cytologically equivocal cases, we adopted the argyrophil technique for staining NOR s (AgNOR) in FNA cytological smears of 56 breast lesions, comprising 31 benign and 25 malignant lesions. Histological correlation was possible in 26 of these cases (17 malignant and 9 benign) and AgNOR scoring was done on paraffin sections of these as well. There was a significant difference between mean AgNOR scores in benign and malignant lesions in the cytological smears (P < 0.001). The AgNOR scores ranged from 2.5 to 5.0 per cell in benign lesions and 5.8 to 17.2 per cell in malignant lesions. None of the cases fell into the gray zone of overlap. One malignant lesion that was cytologically equivocal showed a mean AgNOR score of 6.08. The AgNOR scores on histological sections also showed a statistically significant difference (P < 0.001) between benign and malignant lesions with mean scores ranging from 1.34 to 2.58 dots per cell in benign lesions and scores of 2.42 to 5.28 dots per cell in malignant lesions. However, the scores overlapped in four cases and therefore it was considered unsuitable for routine diagnostic work. From this preliminary study, we conclude that an FNA AgNOR score of 5.0 and less strongly favours a benign lesion whereas a score above 5.0 would be in favour of a malignant lesion. A larger study would be needed to verify our impression that AgNOR scoring can be useful in cytologically equivocal cases.
    Matched MeSH terms: Adenocarcinoma/pathology; Breast/pathology; Breast Neoplasms/pathology*; Carcinoma, Intraductal, Noninfiltrating/pathology; Phyllodes Tumor/pathology; Fibrocystic Breast Disease/pathology; Nucleolus Organizer Region/pathology*; Fibroadenoma/pathology; Carcinoma, Ductal, Breast/pathology
  13. Siar CH, Ng KH
    Br J Oral Maxillofac Surg, 1993 Jun;31(3):183-6.
    PMID: 7685634
    Four cases of either combined occurrence of ameloblastoma and odontogenic keratocyst or a rare keratinising variant of ameloblastoma are presented. The cardinal histomorphologic characteristics are simultaneous occurrence of ameloblastomatous epithelial islands with central keratinisation and multiple keratinising cysts. Immunohistochemically the tumour elements were keratin positive and occasionally S-100 protein and desmin positive. Major differential diagnosis of these neoplasms are discussed.
    Matched MeSH terms: Ameloblastoma/pathology*; Connective Tissue/pathology; Epithelium/pathology; Keratosis/pathology; Mandibular Diseases/pathology; Mandibular Neoplasms/pathology; Maxillary Diseases/pathology; Maxillary Neoplasms/pathology; Odontogenic Cysts/pathology*
  14. Jayaram G, Peh KB
    Diagn Cytopathol, 1995 Nov;13(4):295-9.
    PMID: 8599911
    Three patients presenting with parotid, submandibular, and/or lymph node masses were subjected to fine-needle aspiration cytology. Smears showed dissociated and clustered endothelial cells, eosinophils, lymphocytes, and Warthin Finkeldey giant cells. In two cases a diagnosis of Kimura's disease was suggested from the FNA cytologic smears. In the third case the presence of mononucleate cells with prominent nucleoli led to a suspicion of Hodgkin's disease. Excision biopsy and histopathologic study established a diagnosis of Kimura's disease in all three cases.
    Matched MeSH terms: Angiolymphoid Hyperplasia with Eosinophilia/pathology*; Cell Nucleus/pathology; Cytoplasm/pathology; Endothelium/pathology; Eosinophils/pathology; Hodgkin Disease/pathology; Lymph Nodes/pathology; Lymphocytes/pathology; Plasma Cells/pathology
  15. Subramaniam K, Sheppard MN
    J Forensic Leg Med, 2018 Feb;54:127-129.
    PMID: 29413954 DOI: 10.1016/j.jflm.2018.01.005
    OBJECTIVES: Aortic dissection (AD) can be a challenging diagnosis. At autopsy, the aorta may not be dilated and intimal tears may be missed or found without obvious rupture or haemorrhage. We report our experience of AD at a tertiary referral centre with review of 32 cases and discuss 2 unusual complications.

    METHODS/RESULTS: 32 cases of which 12 females and 20 male and 18 out of 32 cases were aged below 40. All of the cases were examined macroscopically and microscopically. 30 out of 32 cases (93%) died due to rupture associated with the AD. Two unusual complications were proximal extension of AD into left coronary artery (CA) with intramural haematoma blocking the vessel and AD involving the ostium of the right CA resulting in avulsion of the right CA from the aorta. Mode of death in both these cases were myocardial ischemia. Sections of the aorta in all cases confirmed extensive cystic medial degeneration with disorganisation, fragmentation and disappearance of the elastin fibres with increased collagen and smooth muscle nuclear degeneration.

    CONCLUSION: Pathologists should be thorough when examining the aorta, the aortic valve and root in AD. When a rupture site cannot be found it is important to look for unusual complications involving the CAs. Histology plays an important role to corroborate the cause of death.

    Matched MeSH terms: Aneurysm, Dissecting/pathology*; Aorta, Thoracic/pathology*; Aortic Aneurysm/pathology*; Aortic Rupture/pathology*; Coronary Vessels/pathology; Hematoma/pathology; Hemothorax/pathology; Pericardial Effusion/pathology; Forensic Pathology
  16. Loh KB, Rahmat K, Lim SY, Ramli N
    Neurol India, 2011 Mar-Apr;59(2):266-9.
    PMID: 21483130 DOI: 10.4103/0028-3886.79143
    A "Hot Cross Bun" sign on T2-weighted MRI was described as a result of selective loss of myelinated transverse pontocerebellar fibers and neurons in the pontine raphe with preservation of the pontine tegmentum and corticospinal tracts (CST). However, neuropathologic studies showed contradicting results with no sparing of the CST. This is a pictorial and quantitative demonstration of the sign on diffusion tensor imaging and tractography, which provides the imaging evidence that is consistent with neuropathologic findings.
    Matched MeSH terms: Cerebellum/pathology*; Nerve Fibers, Myelinated/pathology*; Neurons/pathology; Pons/pathology*; Pyramidal Tracts/pathology*; Multiple System Atrophy/pathology*
  17. Murty OP
    Am J Forensic Med Pathol, 2009 Jun;30(2):201-3.
    PMID: 19465820 DOI: 10.1097/PAF.0b013e31819d9af5
    Primary cystic tumors of papillary muscles of the heart are extremely rare. Here, one case of unusual cystic tumor in papillary muscle of the heart in a 37-year-old Myanmar migrant worker has been reported. He came to Malaysia 2 weeks before and one morning was found dead in sleep. Autopsy revealed cystic lesion in the papillary muscle of the mitral valve of heart, which was prolapsing into ventricular cavity. The cyst had white-jelly like sticky mucus material. The cyst was present in papillary muscle with slight invasion in septum area; it was lined by cuboidal-columnar epithelium and contained mucinous contents. There was no evidence of an inflammatory reaction in the cyst and in cardiac muscles. In addition to cystic neoplasm, the deceased also had histoplasmosis of the lungs. The case is presented with macroscopic and microscopic photographs of the cyst and histoplasmosis of the lungs. This case is reported because of its rarity, unique position, and unusual appearance.
    Matched MeSH terms: Cysts/pathology*; Heart Septum/pathology; Histoplasmosis/pathology; Cardiomyopathies/pathology*; Papillary Muscles/pathology*; Forensic Pathology
  18. Vollala VR, Nagabhooshana S, Bhat SM, Potu BK, Rodrigues V, Pamidi N
    Rom J Morphol Embryol, 2009;50(1):129-35.
    PMID: 19221659
    During routine dissection classes to undergraduate medical students, we have observed some important anatomic variations in the right upper limb of a 45-year-old cadaver. The anomalies were superficial ulnar artery, persistent median artery, variant superficial palmar arch, third head for biceps brachii, accessory head for flexor pollicis longus, variant insertion of pectoralis major, absence of musculocutaneous nerve, coracobrachialis muscle supplied by lateral root of median nerve and anomalous branching of median nerve in arm and forearm. Although there are individual reports about these variations, the combination of these variations in one cadaver has not previously been described in the literature consulted. Awareness of these variations is necessary to avoid complications during radiodiagnostic procedures or surgeries in the upper limb.
    Matched MeSH terms: Abnormalities, Multiple/pathology*; Arm/pathology; Arteries/pathology; Median Nerve/pathology; Tendons/pathology; Muscle, Skeletal/pathology
  19. Mazlina S, Shiraz MA, Hazim MY, Amran AR, Zulkarnaen AN, Wan Muhaizan WM
    J Laryngol Otol, 2006 Jul;120(7):597-9.
    PMID: 16672089
    Inverted papilloma is a rare, benign tumour representing only 0.5 to 4 per cent of all sinonasal neoplasms; its involvement of the middle ear is extremely rare. We present a case of multicentric inverted papilloma in the sinonasal region and middle ear in a 54-year-old man. The patient later developed neck metastasis secondary to malignant transformation of the inverted papilloma in the middle ear.
    Matched MeSH terms: Ear Neoplasms/pathology*; Ear, Middle/pathology; Maxillary Sinus Neoplasms/pathology*; Neoplasm Recurrence, Local/pathology; Neoplasms, Multiple Primary/pathology; Papilloma, Inverted/pathology*
  20. Ng KH, Siar CH
    Br J Oral Maxillofac Surg, 1993 Oct;31(5):299-303.
    PMID: 8218083
    Seventeen cases are reported of desmoplastic variant of ameloblastoma of the jaws observed during the years 1967-1991. There were 12 females and 5 males, and these consisted of 7 Chinese, 6 Malays, 2 Indians, 1 Sikh and 1 Kadazan. Their ages at diagnosis ranged from 21-60 years with a mean of 36.6 years. There were 10 mandibular and 7 maxillary tumours. Of these, 14 cases involved the anterior segment with extension to the premolar region in 5 cases. 60% of cases were radiologically suggestive of fibro-osseous lesions. The main mode of treatment was resection and 1 case presented with recurrence. The findings of this study were compared with those of previous reports.
    Matched MeSH terms: Ameloblastoma/pathology*; Connective Tissue/pathology; Epithelium/pathology; Mandibular Neoplasms/pathology*; Maxillary Neoplasms/pathology*; Neoplasms, Fibrous Tissue/pathology*
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