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1.
Indian J Pediatr ; 90(10): 969-973, 2023 10.
Article in English | MEDLINE | ID: mdl-37233891

ABSTRACT

OBJECTIVE: To compare the efficacy and tolerability of modified Atkins diet (mAD) and ketogenic diet (KD) among children aged 9 mo to 3 y with epileptic spasms refractory to the first line treatment. METHODS: An open labelled, randomized controlled trial with parallel group assignment was conducted among children aged 9 mo to 3 y with epileptic spasms refractory to the first line treatment. They were randomized to either receive the mAD along with conventional anti-seizure medications (n = 20) or KD with conventional anti-seizure medications (n = 20). Primary outcome measure was proportion of children who achieved "spasm freedom" at 4 wk and 12 wk. Secondary outcome measures were proportion of children who achieved >50% and >90% reduction in spasms at 4 wk and 12 wk, nature and proportion of the adverse effects as per parental reports. RESULTS: Proportion of children achieving spasm freedom [mAD {4 (20%)} vs. KD {3 (15%)}: OR (95% CI) 1.42 (0.27-7.34); P = 0.67], >50% spasm reduction [mAD {3 (15%)} vs. KD {5 (25%)}: OR (95% CI) 0.53 (0.11-2.59); P = 0.63] and >90% spasm reduction [mAD {4 (20%)} vs. KD {2 (10%)}: OR (95% CI) 2.25 (0.36-13.97); P = 0.41] was comparable between the two groups at 12 wk. The diet was well tolerated in both the groups with vomiting and constipation being the most common reported adverse effect. CONCLUSIONS: mAD is an effective alternative to KD in the management of children with epileptic spasms refractory to first line treatment. However, further studies with adequately powered sample size and longer follow-up are required. TRIAL REGISTRATION: CTRI/2020/03/023791.


Subject(s)
Diet, High-Protein Low-Carbohydrate , Diet, Ketogenic , Drug-Related Side Effects and Adverse Reactions , Spasms, Infantile , Child , Humans , Infant , Diet, Ketogenic/adverse effects , Diet, Carbohydrate-Restricted , Spasms, Infantile/drug therapy , Treatment Outcome
3.
Indian J Pathol Microbiol ; 64(4): 802-805, 2021.
Article in English | MEDLINE | ID: mdl-34673609

ABSTRACT

Collision tumors are characterized by occurrence of two or more histologically distinct tumor types at the same anatomic site. Collision tumors have been reported in various organs, such as esophagus, stomach, colon, kidney, lung, skin, thyroid, breast, ovary and uterus. Uterine collision tumors of epithelial and mesenchymal origin are rare and often underrecognized. We report a rare concurrent occurrence of endometrial stromal sarcoma and endometrioid adenocarcinoma in a 65-year-old female. It is important to differentiate collision tumors from carcinosarcoma due to impact on clinical management and prognosis. Extensive gross sampling and careful morphological examination aided by immunohistochemical studies is necessary for the diagnosis of this rare entity. This case report aims to increase the awareness of this rare pathological entity with discussion on the management issue based on review of literature. This is the first case in Indian literature to the best of our knowledge.


Subject(s)
Carcinoma, Endometrioid/pathology , Endometrial Neoplasms/pathology , Sarcoma, Endometrial Stromal/pathology , Aged , Carcinoma, Endometrioid/diagnosis , Carcinoma, Endometrioid/surgery , Endometrial Neoplasms/diagnosis , Endometrial Neoplasms/surgery , Female , Humans , Immunohistochemistry , Sarcoma, Endometrial Stromal/diagnosis , Sarcoma, Endometrial Stromal/surgery
4.
Arq. bras. neurocir ; 40(2): 186-189, 15/06/2021.
Article in English | LILACS | ID: biblio-1362256

ABSTRACT

The most common mixed glioma encountered in routine surgical practice is oligoastrocytoma (OA); however, its is currently considered a vanishing entity. The 2016 classification of the World Health Organization (WHO) discourages the diagnosis of tumors as mixed glioma. The recommendations are that diffuse gliomas, including those withmixed or ambiguous histological features, should be subjected tomolecular testing. Dual-genotype OAs are not yet a distinct entity or variant in the classification. We report a case ofmixed glioma: a pleomorphic xanthoastrocytoma (PXA)mixed with an oligodendroglioma. The immunohistochemistry (IHC) pattern of isocitrate dehydrogenase 1 (IDH1) negativity with retained nuclear expression of the alpha-thalassemia x-linked intellectual disability syndrome (ATRX) protein, and 1p19q co-deletion negativity in both the components enabled its identification as a mixed glioma rather than a collision tumor. To the best of our knowledge, the case herein presented is the fourth case of PXA with oligodendroglioma. Out of the other three reported cases, only one was of a collision tumor with a dual genotype, and the other two showed similar molecular signatures in both components. The present article discusses the histological, immunohistochemical and molecular features of the aforementioned case.


Subject(s)
Humans , Male , Adult , Oligodendroglioma/surgery , Astrocytoma/surgery , Brain Neoplasms/therapy , Neoplasms, Multiple Primary/surgery , Oligodendroglioma/pathology , Oligodendroglioma/diagnostic imaging , Astrocytoma/pathology , Temporal Lobe/surgery , Aconitate Hydratase/genetics , Chromosomes, Human, Pair 1 , Chromosomes, Human, Pair 19 , Chromosome Deletion , Telomerase/genetics , Craniotomy/methods
6.
Indian J Pathol Microbiol ; 56(4): 440-2, 2013.
Article in English | MEDLINE | ID: mdl-24441243

ABSTRACT

A variety of lymphoma types have been reported in patients being treated with anticonvulsant therapy. Non-Hodgkin lymphomas have been reported twice as frequently as Hodgkin lymphomas. Association of nodular lymphocyte predominant Hodgkin lymphoma (NLPHL) with dilantin therapy is extremely uncommon. We report a case of Hodgkin lymphoma in a 25-year-old male patient who had been treated with diphenylhydantoin sodium for generalized tonic clonic seizures for 15 years. Patient presented with left cervical and axillary lymphadenopathy persisting for more than 2 years after cessation of treatment with diphenylhydantoin. Computerized tomography scan of thorax, abdomen and pelvis revealed no significant lymphadenopathy or any organomegaly. Diagnosis of NLPHL was made on excision biopsy of the cervical lymph node. Although the association between diphenylhydantoin therapy and the development of immunosuppression and lymphoma is well-documented, the role of the drug in the etiology of these disorders is still controversial.


Subject(s)
Anticonvulsants/adverse effects , Axilla/pathology , Hodgkin Disease/diagnosis , Lymphatic Diseases/etiology , Neck/pathology , Phenytoin/adverse effects , Adult , Anticonvulsants/therapeutic use , Hodgkin Disease/pathology , Humans , Lymphatic Diseases/pathology , Male , Pelvis/diagnostic imaging , Phenytoin/therapeutic use , Radiography, Abdominal , Radiography, Thoracic , Tomography, X-Ray Computed
7.
Appl Opt ; 51(19): 4554-62, 2012 Jul 01.
Article in English | MEDLINE | ID: mdl-22772130

ABSTRACT

In this paper the effect of uniform magnetic field B on the temperature and temperature profile of the diffusion flame is investigated using lensless Fourier transform digital holographic interferometry. The evaluation of temperature profile reveals that the width of flame as well as the maximum value of temperature inside the flame is increased.

8.
Appl Opt ; 51(16): 3228-35, 2012 Jun 01.
Article in English | MEDLINE | ID: mdl-22695554

ABSTRACT

In this paper, experimental investigations and analysis is presented to measure the temperature and temperature profile of gaseous flames using lensless Fourier transform digital holographic interferometry. The evaluations of the experimental results give the accuracy, sensitivity, spatial resolution, and range of measurements to be well within the experimental limits. Details of the experimental results and analysis are presented.

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