Dillip K Muduly
All India Institute of Medical Sciences
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Publication
Featured researches published by Dillip K Muduly.
Indian Journal of Palliative Care | 2011
Dillip K Muduly; S. V. S. Deo; Ts Subi; Ashwin Anand Kallianpur; Nootan Kumar Shukla
Malignant pleural effusion (MPE) usually presents in the disseminated and advanced stage of malignancy. Dyspnea is the debilitating symptom which needs palliation in these patients. Various modalities are available in the management of MPE. Careful consideration of the patients expected survival and quality of life is needed when deciding the optimum treatment modality in such patients. In this article, different modalities of the palliative management of MPE are discussed with an attempt to derive a treatment algorithm for the management of MPE.
Journal of Cancer Research and Therapeutics | 2013
Ashwin Anand Kallianpur; Rakesh K. Gupta; Dillip K Muduly; Arvind Kapali; Kiran Subbarao
Primary osteogenic sarcomas of the breast are exceptionally uncommon. We describe such a case occurring in a 50 year-old woman who presented with a large painful mass in her left breast. Simple mastectomy of the left breast was performed. Microscopical and immunohistochemical findings established the diagnosis of primary osteogenic sarcoma. Similar to extremity osteosarcoma, adjuvant adriamycin and cisplatin based chemotherapy and external beam radiotherapy was given to the present case. She remained well 57 months later, without tumor recurrence. The current article made a literature search proving the rarity of this lesion type and discusses in detail the diagnostic implications and the treatment of this rare site tumor entity.
Indian Journal of Palliative Care | 2011
Parveen Yadav; Nml Manjunath; S. V. S. Deo; Nootan Kumar Shukla; Prashant Durgapal; Dillip K Muduly
Carcinoma of the cervix is the most common malignancy among women in India. Although metastatic disease is common, metastasis to breast is rare. A limited number of case reports are published in the world literature. Most of the previous reports of metastatic cervical carcinoma to breast are either autopsy series or widely disseminated disease where no treatment options were available. A rare case of cervical carcinoma presenting as metastasis in breast is reported here where palliative mastectomy improved the general condition of the patient. A female patient aged 58 years was diagnosed and treated for cervical carcinoma, FIGO stage 2B. Four months after the treatment which included both external beam and intracavitory radiotherapy, the patient presented with breast and lung metastasis. Palliative mastectomy was done which improved the general condition of the patient. Metastatic carcinoma of the cervix can present as a case of breast carcinoma. In an appropriate setting, this possibility should be kept in mind. Palliative mastectomy should be offered for patients of cervical carcinoma with metastasis to breast when needed.
Indian Journal of Palliative Care | 2010
As Kapali; Mandeep Singh; S. V. S. Deo; N. K. Shukla; Dillip K Muduly
Metastatic phyllodes tumor has very few treatment options. Phyllodes tumor in metastatic setting has limited role of surgery, radiotherapy and chemotherapy or combined treatment. Most of the patients receive symptomatic management only. We present a case of metastatic phyllodes tumor managed with aggressive margin negative resection of primary tumor leading to palliation of almost all the symptoms, which eventually led to improved quality of life and probably to improved survival. The improved quality of life was objectively assessed with Hamilton depression rating scale. Surgery may be the only mode of palliation in selected patients that provides a better quality of life and directly or indirectly may lead to improved survival.
Case Reports | 2017
Ashish Jakhetiya; Nootan Kumar Shukla; Dillip K Muduly; Shashank Sharad Kale
Extraskeletal orbital mesenchymal chondrosarcoma (MC) is an extremely rare and highly aggressive tumour. It has characteristic radiological features and pathognomic histological biphasic pattern. Radical resection with negative margins is the mainstay of treatment; role of adjuvant chemotherapy and radiotherapy is yet not well defined. We report a rare case of 18-year-old man who was diagnosed to have orbital MC. He presented with locally advanced disease with no vision in the affected eye. He underwent right orbital exenteration; a transcranial intradural approach was used to divide the optic nerve, and the temporalis muscle flap was utilised to fill the exenterated orbit. Though optic nerve involvement is rare in orbital MCs, a transcranial approach may be used effectively to avoid traction on optic chiasma and ensure margin-free resection in case of optic nerve involvement up to orbital apex. Unfortunately, prognosis remains dismal in MCs despite treatment.
Orbit | 2011
Dillip K Muduly; S. V. S. Deo; Nootan Kumar Shukla; Rajni Yadav; Ashwin Anand Kallianpur; Subrat Samantara
Basal cell adenocarcinoma (BCAC) is a recently described rare salivary gland tumor. They are locally invasive and destructive tumors with rare incidence of metastasis. BCAC most commonly occur in the parotid gland followed by the submandibular and other minor salivary glands. The primary management of these tumors is surgery with or without adjuvant radiotherapy. Lacrimal gland is a very rare location of BCAC; only one case has been reported in English literature. We report a case of recurrent basal cell adenocarcinoma of lacrimal gland in a 75-year-old female. She had past history of local excision of a tumor in the lacrimal gland of same side 10 years back, details of which were not available with the patient. We discuss about the case and review the literature about treatment modality in basal cell adenocarcinoma.
Journal of Cancer Research and Therapeutics | 2012
Dillip K Muduly; Ashwin Anand Kallianpur; Sv Suryanarayana Deo; Nootan Kumar Shukla; Aravind S Kapali; Rajni Yadav
Primary leiomyosarcomas rarely arise from epididymis. But they are the most common histopathological types of sarcoma arising from the epididymis. Primary epididymal leiomyosarcoma occurs usually in older patients. We report a young patient of 35 years presenting with leiomyosarcoma of left epididymis. He did not have any metastasis and underwent left high inguinal orchiectomy. He is on regular follow-up and disease free for last two years.
Tropical gastroenterology : official journal of the Digestive Diseases Foundation | 2012
Dillip K Muduly; S. V. S. Deo; Nootan Kumar Shukla; Manjunath Nm; Durgapal P; Ashwin Anand Kallianpur
Indian Journal of Surgery | 2015
Subodh Kumar; Virinder Kumar Bansal; Dillip K Muduly; Pawan Sharma; Mahesh C. Misra; Sunil Chumber; Saraman Singh; D. N. Bhardwaj
Indian Journal of Cancer | 2015
Ashwin Anand Kallianpur; As Kapali; N. K. Shukla; S. V. S. Deo; Dillip K Muduly; Rajni Yadav