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1.
J Pediatr Endocrinol Metab ; 35(8): 998-1002, 2022 Aug 26.
Article in English | MEDLINE | ID: mdl-35700451

ABSTRACT

OBJECTIVES: Fetal adrenals are one of the main organs responsible for maturation and survival. Extant literature is not clear about whether second trimester fetal adrenals are capable of synthesizing secreting aldosterone. METHODS: We have taken 20 adrenals from fetuses of intrauterine death cases. None of the fetuses had any external malformations and obstetric history was unremarkable. The organs were weighed and homogenized. The supernatant was used for aldosterone estimation by ELISA. RESULTS: We consistently detected aldosterone in all the cases including second trimester. However, we did not see any correlation between aldosterone concentration and gestational age. It is striking to note that there are wide variations in the tissue levels of aldosterone across different gestational ages and also same period. CONCLUSIONS: Tissue aldosterone levels in second trimester can be possibly induced by stress preceding intrauterine deaths. It is possible that functional status of adrenal is different in intrauterine death cases as opposed to elective abortions in second trimester.


Subject(s)
Aldosterone , Fetus , Adrenal Glands , Female , Gestational Age , Humans , Pregnancy
3.
Med Hypotheses ; 144: 110209, 2020 Nov.
Article in English | MEDLINE | ID: mdl-33254516

ABSTRACT

There is a significant difference between COVID 19 associated mortality between different countries. Generally the number of deaths per million population are higher in the developed countries despite better health care efficiency, drinking water quality and expected healthy life span (HALE) at the time of birth. Developing and underdeveloped countries on the other hand have lower mortality even with higher rural and slum populations along with incidence of diarrhea because of lack of sanitation. We analyzed data from 122 countries out of which 80 were high or upper middle income and 42 were low or low middle income countries. There was statistically significant positive correlation between COVID 19 deaths /million population and water current score, health efficiency, and HALE. Statistically significant negative correlation was observed with % rural population and fraction of diarrhea because of inadequate sanitation for all ages. Moreover analysis of 51 countries showed that there is significant negative correlation between COVID 19 deaths /million population and proportion of total population living in slums. We propose that high microbial exposure particularly gram negative bacteria can possibly induce interferon type I which might have a protective effect against COVID 19 since the countries with less mortality also tend to have lack of sanitation and high incidence of attendant diseases. So, far none of the predictive models have taken into account immune status of populations engendered by environmental microbial exposure or microbiome. There might be a need to look at dynamics of COVID 19 pandemic using immune perspective. The approach can potentially inform better policies including interventions.


Subject(s)
COVID-19/microbiology , COVID-19/mortality , Microbiota , Pandemics , SARS-CoV-2 , Bacterial Infections/immunology , Biodiversity , COVID-19/immunology , Developing Countries , Environmental Microbiology , Health Status Disparities , Humans , Interferon Type I/immunology , Microbiota/immunology , Models, Biological , Poverty , Rural Population
4.
J Exp Clin Cancer Res ; 38(1): 175, 2019 Apr 25.
Article in English | MEDLINE | ID: mdl-31023373

ABSTRACT

BACKGROUND: Head and neck squamous-cell carcinoma (HNSCC) ranks sixth among cancers worldwide. Though several molecular mechanisms of tumor initiation and progression of HNSCC are known, others remain unclear. Significance of p38/MAPKAPK2 (Mitogen-activated protein kinase-activated protein kinase-2) pathway in cell stress and inflammation is well established and its role in tumor development is being widely studied. METHODS: We have elucidated the role of MAPKAPK2 (MK2) in HNSCC pathogenesis using clinical tissue samples, MK2-knockdown (MK2KD) cells and heterotropic xenograft mice model. RESULTS: In patient-derived tissue samples, we observed that MK2 is reproducibly overexpressed. Increased stability of cyclin-dependent kinase inhibitor 1B (p27), mitogen-activated protein kinase phosphatase-1 (MKP-1) transcripts and decreased half-life of tumor necrosis factor-alpha (TNF-α) and vascular endothelial growth factor (VEGF) transcripts in MK2KD cells suggests that MK2 regulates their transcript stability. In vivo xenograft experiments established that knockdown of MK2 attenuates course of tumor progression in immunocompromised mice. CONCLUSION: Altogether, MK2 is responsible for regulating the transcript stability and is functionally important to modulate HNSCC pathogenesis.


Subject(s)
Cell Proliferation/genetics , Inflammation/genetics , Intracellular Signaling Peptides and Proteins/genetics , Protein Serine-Threonine Kinases/genetics , Squamous Cell Carcinoma of Head and Neck/genetics , Animals , Cyclin-Dependent Kinase Inhibitor p27/genetics , Dual Specificity Phosphatase 1/genetics , Humans , Inflammation/pathology , Mice , Proliferating Cell Nuclear Antigen/genetics , RNA, Messenger/genetics , Squamous Cell Carcinoma of Head and Neck/pathology , Tumor Necrosis Factor-alpha/genetics , Vascular Endothelial Growth Factor A/genetics , Xenograft Model Antitumor Assays
5.
J Cancer Res Ther ; 14(3): 719-721, 2018.
Article in English | MEDLINE | ID: mdl-29893351

ABSTRACT

Chondrosarcoma is a rare malignant tumor of cartilage commonly arising in the pelvis, proximal femur, and humerus, but quite uncommon in the small bones of the hand. Although limited surgical procedures such as curettage are mentioned as a management option in low-grade chondrosarcomas, they tend to have a high rate of recurrences. Hence, wide excision is recommended as a treatment option even in low-grade chondrosarcomas of the hand.


Subject(s)
Bone Neoplasms/surgery , Chondrosarcoma/surgery , Metacarpal Bones/surgery , Adult , Bone Neoplasms/diagnosis , Chondrosarcoma/diagnosis , Humans , Male , Metacarpal Bones/pathology , Prognosis , Young Adult
6.
J Lab Physicians ; 10(1): 106-108, 2018.
Article in English | MEDLINE | ID: mdl-29403216

ABSTRACT

Enterobius vermicularis is an intestinal nematode commonly affecting children worldwide. Its transmission is by feco-oral route. Meckel's diverticulitis due to E. vermicularis infestation is an extremely rare presentation. An 11-year-old boy presented with acute abdomen. During surgery inflamed Meckel's diverticulum (M.D) was seen. Histopathology examination of specimen revealed E. vermicularis. Till date, only one case of E. vermicularis infestation of M.D is reported around five decades ago. This histopathological confirmation is extremely important as the required treatment (Mebendazole) of the infected case along with household contacts can prevent the spread of infection and may avoid surgery in known contacts.

7.
J Lab Physicians ; 8(2): 126-8, 2016.
Article in English | MEDLINE | ID: mdl-27365925

ABSTRACT

Heterotopic pancreatic tissue in the gall bladder is an uncommon incidental finding in most cases. We hereby describe the case of a 45-year-old woman who presented with symptoms of acalculous cholecystitis. Pathological examination detected heterotopic pancreatic tissue, pseudopyloric metaplasia, and adenomyomatous hyperplasia in the gall bladder. This is a rare combination of three entities which is being reported for the first time. This case emphasizes that heterotopic pancreas might be the causative factor for cholecystitis.

8.
Pol J Radiol ; 81: 256-60, 2016.
Article in English | MEDLINE | ID: mdl-27298654

ABSTRACT

BACKGROUND: Paediatric renal cell carcinoma (RCC) is a rare neoplasm which differs significantly in its clinico-pathological behaviour from the adult variant. The clear cell variant constitutes a relatively small histological subset of this neoplasm. CASE REPORT: We present a very unusual, pathologically proven case of clear cell variety of pediatric RCC which showed invasion into the pelvicalyceal system with contiguous extension up to the urinary bladder. Such a novel manifestation of paediatric RCC has not been described previously in literature. A relevant review of literature is included. CONCLUSIONS: The aggressive biological behaviour of the paediatric RCC in our case and the consequent atypical imaging findings are distinctly unusual. These findings may represent a new aggressive variant of this rare neoplasm. The radiologist and clinician should be aware of these novel manifestations of paediatric clear cell RCC.

9.
J Cancer Res Ther ; 11(3): 646, 2015.
Article in English | MEDLINE | ID: mdl-26458605

ABSTRACT

Lipoma arborescens is a rare lesion wherein abnormal proliferation of adipocytes in the subsynovial region is seen. Whether it is neoplastic or not is still not entirely clear. Usually, Lipoma arborescens is seen unilaterally around knee joint but it can also be seen around tendon sheaths or bursa in adults. Multiple lesions are also reported. Involvement of wrist is extremely rare. We are presenting a case with bilateral wrist involvement by Lipoma arborescens which to the best of our knowledge is first one in English literature. There are a host of co-morbid/associated conditions reported with Lipoma arborescens out of which chronic irritation and inflammation appears to be most significant. We are proposing a novel perspective on etiopathogenesis of Lipoma arborescens based on extant understanding of cellular differentiation and information gleaned from fetal autopsies. The new perspective also explains the predilection for knee joint.


Subject(s)
Lipoma/diagnosis , Neoplasms, Multiple Primary/diagnosis , Soft Tissue Neoplasms/diagnosis , Wrist/pathology , Adult , Humans , Lipoma/surgery , Male , Neoplasms, Multiple Primary/surgery , Soft Tissue Neoplasms/surgery , Wrist/surgery
10.
J Cancer Res Ther ; 11(3): 652, 2015.
Article in English | MEDLINE | ID: mdl-26458634

ABSTRACT

We are presenting two unique cases of lymphangiomatosis without visceral and bony involvement and critically discussing the nomenclature used in the extant literature. The first case was a 12-year-old boy with ill-defined mass on the right cheek extending into the ipsilateral orbit leading to conjunctival lesion. The second case was of a 14-week-old infant showing diffuse swelling on nape of the neck. In addition there were raised patches on dorsal aspects of bilateral hands and feet. The biopsies from all the lesions showed similar histopathological features consistent with lymphangiomatosis. We propose that the term lymphangiomatosis should be used only in cases with histological features of lymphangiomatosis. The term should not be used in cases of multiple lymphangiomas. We conclude that the lesions clinically diagnosed as lymphangioma may turn out to be lymphangiomatosis. Extensive lymphangiomatosis without visceral or bony involvement may lead to intrauterine death.


Subject(s)
Lymphangioma/diagnosis , Lymphangioma/physiopathology , Biopsy , Child , Humans , Infant , Lymphangioma/diagnostic imaging , Male , Tomography, X-Ray Computed
11.
J Cancer Res Ther ; 11(3): 659, 2015.
Article in English | MEDLINE | ID: mdl-26458668

ABSTRACT

Mucinous tubular and spindle cell carcinoma (MTSCC) is a rare and unusual variant of renal cell carcinoma (RCC). It is important to differentiate this from the other variants particularly papillary RCC since MTSCC is generally low-grade, has low malignant potential and favorable prognosis. We are reporting a 40-year-old female presenting with right flank pain and well-circumscribed renal mass confined to the lower pole. Tumor consisted of tubules and cords separated by pale mucinous material in some areas, whereas other areas showed dense cellularity without significant mucin. The tumor cells were cuboidal or spindle and did not show significant atypical features. The patient underwent nephrectomy and is asymptomatic clinically and radiologically after 2 years.


Subject(s)
Adenocarcinoma, Mucinous/diagnosis , Adenocarcinoma/diagnosis , Carcinoma, Renal Cell/diagnosis , Kidney Neoplasms/diagnosis , Sarcoma/diagnosis , Adenocarcinoma/surgery , Adenocarcinoma, Mucinous/surgery , Adult , Carcinoma, Renal Cell/surgery , Female , Humans , Kidney Neoplasms/surgery , Sarcoma/surgery
12.
J Cancer Res Ther ; 11(3): 661, 2015.
Article in English | MEDLINE | ID: mdl-26458678

ABSTRACT

Being one of the commonest tumors of the female genital tract during the reproductive years, the leiomyoma uteri expectedly demonstrates a wide spectrum of histological variations. However, heterologous tissue differentiation is a rare finding and frank bone formation is even rarer. The factors that lead to heterologous tissue formation in a leiomyoma are subject to speculation. This is a rare case report and possibly the first, on the formation of pure mature bone in a uterine leiomyoma.


Subject(s)
Calcinosis/diagnostic imaging , Leiomyoma/diagnostic imaging , Metaplasia/diagnostic imaging , Uterine Neoplasms/diagnostic imaging , Calcinosis/surgery , Female , Humans , Leiomyoma/surgery , Metaplasia/surgery , Middle Aged , Ultrasonography , Uterine Neoplasms/surgery , Uterus/diagnostic imaging , Uterus/pathology
14.
J Cancer Res Ther ; 11(4): 1027, 2015.
Article in English | MEDLINE | ID: mdl-26881600

ABSTRACT

Renal cell carcinoma, unclassified constitute about 3-4% of all renal carcinomas. It essentially is a tumor where more than morphological variants or subtypes are seen in a single tumor. Usually there is a mixture of 2-3 different types. However, in this particular case there were at least 5 different types of morphological patterns in a single tumor including areas of so-called rhabdoid differentiation. The patient underwent nephrectomy and has been asymptomatic for the last 3.5. years. To the best of our knowledge, this is the first case of its own kind in the published literature.


Subject(s)
Biomarkers, Tumor/metabolism , Carcinoma, Renal Cell/classification , Kidney Neoplasms/classification , Carcinoma, Renal Cell/metabolism , Carcinoma, Renal Cell/pathology , Carcinoma, Renal Cell/surgery , Cell Differentiation , Humans , Kidney Neoplasms/metabolism , Kidney Neoplasms/pathology , Kidney Neoplasms/surgery , Male , Middle Aged , Nephrectomy
15.
Turk Patoloji Derg ; 30(3): 195-200, 2014.
Article in English | MEDLINE | ID: mdl-24994612

ABSTRACT

OBJECTIVE: To present and critically examine the spectrum of chondrocutaneous branchial remnants or accessory pinna, including rare case of bilateral cervical lesions, and to explain the basis of the biological behavior. MATERIAL AND METHOD: Five cases of pediatric chondrocutaneous branchial remnants or accessory pinna were included. The ratios of the longest dimensions of the external ear to that of the accessory tragus/chondrocutaneous branchial remnants were calculated. RESULTS: The size and rate of growth of chondrocutaneous branchial remnants or accessory pinna were found to be inversely proportional to the distance between the lesions and the normal pinna. CONCLUSION: The current literature and norms of terminology dictate that two different terminologies for lesions that are essentially histologically identical should be avoided. Chondrocutaneous branchial remnants, accessory pinna/tragus and chondroid/ cartilaginous choristomas are identical lesions with similar pathogeneses and should be referred to as choristomas.


Subject(s)
Cartilage , Choristoma , Ear Auricle/pathology , Face/pathology , Neck/pathology , Child , Child, Preschool , Female , Humans , Infant , Male , Skin/pathology
16.
J Midlife Health ; 5(2): 55-61, 2014 Apr.
Article in English | MEDLINE | ID: mdl-24970982

ABSTRACT

OBJECTIVE: The aim of the study was to generate baseline data for indications of gynecological surgeries, and to assess route of surgery and histopathology correlation in women undergoing major gynecological surgery in a rural tertiary level teaching hospital in India. MATERIALS AND METHODS: Surgical indications, route of surgery and histopathology findings were reviewed and analyzed retrospectively, in 922 patients (≥35 years age) who underwent gynecological surgery at Dr. Rajendra Prasad Government Medical College, Kangra, Himachal Pradesh, India from January 1, 2011 to May 31, 2013. RESULTS: Of 922 surgeries, 65 had malignancy (7%). Pelvic organ prolapse (POP) (32.3%) and leiomyoma uterus (29%) were two most common benign indications for hysterectomy. Ovarian tumors were present in 13% (25% of these were malignant). Postmenopausal bleeding (PMB) was seen in 5.5% (55% of these were malignant). CONCLUSIONS: All except 10% surgeries were done in the absence of definite histopathology diagnosis that is dysfunctional uterine bleeding (n = 42 [45%]), chronic pelvic pain/severe dysmenorrhea (n = 34 [36%]) and recurrent PMB (n = 17 [19%]). Majority of surgeries had histopathological correlation except for six cases (0.6%) of malignancy, which were missed on initial work-up. Majority of the surgeries were done abdominally. In rural areas of developing countries poverty, lack of regular follow-up, resource constraints and lack of technical skills (with respect to laparoscopic/robotic surgeries) pose major challenge in providing quality health care.

18.
J Obstet Gynaecol India ; 64(2): 148-9, 2014 Apr.
Article in English | MEDLINE | ID: mdl-24757346
19.
J Pediatr Adolesc Gynecol ; 27(3): e69-71, 2014 Jun.
Article in English | MEDLINE | ID: mdl-24119657

ABSTRACT

BACKGROUND: Uterine angioleiomyoma is a very rare gynecologic tumor; only a few such cases have been reported to date and we have found no such tumor reported in an adolescent girl. CASE: We report the case of a uterine angioleiomyoma in an adolescent girl. It presented as a huge abdomino-pelvic mass. The girl had severe menorrhagia and severe anemia. Intra-operatively no distinct planes were found between myoma and myometrium. Due to severe hemorrhage, she underwent sub-total abdominal hysterectomy. SUMMARY AND CONCLUSION: Uterine angioleiomyoma is an extremely rare tumor since only 16 such cases have been reported to date. Its appearance in an adolescent girl seems to be the first case of its kind. So it is being reported not only to familiarize the managing physicians with the possibility of such a tumor and its variable presentation, but also to highlight the need for inclusion of this tumor in WHO classification of tumors of the female genital tract.


Subject(s)
Angiomyoma/diagnosis , Uterine Neoplasms/diagnosis , Anemia/etiology , Angiomyoma/complications , Female , Humans , Hysterectomy , Menorrhagia/etiology , Uterine Neoplasms/complications , Young Adult
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