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Dive into the research topics where Chandralekha Tampi is active.

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Featured researches published by Chandralekha Tampi.


Digestive Surgery | 2004

Calcitonin-Secreting Tumor of the Pancreas

Prashant Mullerpatan; Shashank R. Joshi; R. Shah; Chandralekha Tampi; Vatsala M. Doctor; Palepu Jagannath; Irvin M. Modlin

Pancreatic endocrine tumors (PETs) are unusual tumors arising from cells belonging generically to the amine precursor uptake and decarboxylation systems. We present a case of a calcitonin-secreting PET in a 56-year-old female who presented with watery diarrhea, dehydration and hypokalemia. Investigation revealed hypercalcemia, hyperphosphatemia, hypercalcitonemia and a well-defined mass in the head of the pancreas on CT scan. Following a pancreaticoduodenectomy her serum calcitonin levels returned to normal and diarrhea disappeared. The identification of this particularly rare presentation of a calcitonin-secreting PET provides the opportunity to examine this pathological entity within the context of the very few previously reported instances of this disease.


Pancreatology | 2006

Microcystic serous cystadenoma of the pancreas: a report of two cases with one of diffuse presentation

Chandralekha Tampi; Prashant Mullerpatan; R. Shah; Palepu Jagannath; Arthur Zimmermann

Microcystic adenoma or serous cystadenoma is an uncommon tumor and accounts for 1–2% of the exocrine neoplasms of the pancreas. Usually unifocal, they present as single, large, well-demarcated multiloculated cystic tumors, ranging in size from 1 to 25 cm. Multifocal variants or diffuse serous cystadenomas are extremely rare. We present 2 cases of which 1 is a diffuse variant affecting the body, tail and part of the neck of the pancreas. In both the patients the tumors were detected incidentally. We highlight on the diffuse variant in view of its rarity and present a review of literature. In this case the entire body and tail of the pancreas was spongy replaced by multicystic lobules and hyalinized fibrocollagenous stroma. The cysts were lined by low cuboidal glycogen containing bland cells. Such a unique presentation wherein the entire body and tail of the pancreas is replaced with multiple cysts is a diffuse presentation of microcystic adenoma and a search through literature revealed only 7 such cases among the 15 cases with multifocal presentation reported.


International Journal of Gastrointestinal Cancer | 2005

HPV-associated carcinoma of esophagus in the young: a case report and review of literature.

Chandralekha Tampi; Sandhya Pai; Vatsala M. Doctor; S. Plumber; Palepu Jagannath

Esophageal carcinoma (EC) is rare in the younger age group, with only 15 cases reported in world literature. It is even rarer for an etiological agent to be implicated.A case of a 15-yr-old boy with squamous cell carcinoma of the esophagus is reported. Human papillomavirus (HPV) 16 DNA sequences were detected in the neoplasm and the adjacent mucosa by polymerase chain reaction followed by restriction fragment length polymorphism (PCR-RFLP). The adjacent mucosa also showed virus-induced changes.


Indian Journal of Pathology & Microbiology | 2012

In search of the rainbow: Colored inks in surgical pathology

Chandralekha Tampi

INTRODUCTION Although surgical pathologists are aware of the multiple advantages that coloured inks contribute to surgical pathology practice, these coloured inks are not available in India and importing them is not a viable proposition. A systematic search for locally available coloring agents was done, and resulted in identifying specific shades within a popular set of childrens hobby colors of a particular brand. They retain their bright distinct colors on paraffin blocks and sections. These paints are available all over India, and are cheap, safe, and easy to use. Coloring gross specimen excision margins with different colors, adds precision to margin examination. It allows three-dimensional microscopic reconstruction of the tumor vis-a-vis its various neighboring anatomic structures. It allows postoperative comparison of tissue planes predicted by preoperative imaging. It maintains orientation of grossed and dissected specimens, enabling the pathologist to re-visit the grossed specimen, if required, and confidently allows further sampling if necessary. AIM A systematic search for indigenous coloring agents was carried out, which included the dyes used in the histopathology laboratory, gelatin, commercially available paints, including acrylic paints and inks. RESULTS The study identified specific shades within a brand of acrylic colors that are easily available and simple to use, with good results on microscopic examination. CONCLUSION Colored inks lend precision to margin examination. A set of easily procurable colors are available in our country, which are easy to use, with distinct bright colors, safe, and reliable.


Indian Journal of Medical and Paediatric Oncology | 2014

Interobserver variation is a significant limitation in the diagnosis of Burkitt lymphoma.

Swapnil Ulhas Rane; Tanuja Shet; Epari Sridhar; Sanica Bhele; Vaishali Gaikwad; Shubhangi Vinayak Agale; Sweety Shinde; Daksha Prabhat; Gwendolyn Fernandes; Meenal Hastak; Chandralekha Tampi; Swati Narurkar; Keyuri Patel; Cv Madiwale; Ketki Shah; Laxmi Shah; Satyakam Sawaimoon; Purnima Lad

Context: The pathology of classic Burkitt lymphoma (BL) remains a challenge despite being a well-defined entity, in view of the significant overlap with atypical BL and B-cell lymphoma intermediate between DLBL (diffuse large B cell lymphoma) and BL. They are difficult to be segregated in resource-limited setups which lack molecular testing facilities. This is further affected by interobserver variability and experience of the reporting pathologist. Aims: The aim of our study was to quantitate variability among a group of pathologists with an interest in lymphomas (albeit with variable levels of experience) and quantitate the benefit of joint discussions as a tool to increase accuracy and reduce interobserver variability of pathologists, in the diagnosis of BL in a resource-limited setup. Materials and Methods: A set of 25 non-Hodgkin lymphoma cases in which a diagnosis of BL was entertained were circulated to 14 participating pathologist within the Mumbai lymphoma study group. A proforma recorded the morphologic and immunohistochemical features perceived during the initial independent diagnosis followed by a consensus meeting for discussion on morphology and additional information pertinent to the case. Statistical analysis and Results: The concordance was poor for independent diagnosis among all the pathologists with kappa statistics (±SE) of 0.168 (±0.018). Expert lymphoma pathologists had the highest (albeit only fair) concordance (kappa = 0.373 ± 0.071) and general pathologists the lowest concordance (kappa = 0.138 ± 0.035). Concordance for morphological diagnosis was highest among expert lymphoma pathologists (kappa = 0.356 ± 0.127). Revision of diagnoses after consensus meeting was highest for B-cell lymphoma intermediate between DLB and BL. To conclude, interobserver variation is a significant problem in BL in the post WHO 2008 classification era. Experience with a larger number of cases and joint discussion exercises such as the one we conducted are needed as they represent a simple and effective way of improving diagnostic accuracy of pathologists working in a resource-limited setup.


International Journal of Surgery Case Reports | 2016

Ileal duplication cyst in the elderly complicated by appendicitis: A rare case report and review of literature

Kamal Sunder Yadav; Priyanka Akhilesh Sali; Bhushan Bhole; Chandralekha Tampi; Hitesh Mehta

Highlights • Duplication cysts seen commonly in the pediatric population is a rare entity in the elderly.• Surgical resection is necessary due to possible complications.• Laparoscopic management aids early recovery and minimum morbidity.


Indian Journal of Surgery | 2012

Pathology for the HPB Surgeon.

Chandralekha Tampi

Optimal care of a patient implies a good professional understanding between all the medical personnel involved in that patient’s care. Similarly a basic understanding of the areas where surgery and pathology interact would go a long way, in clarifying the disease process in the patient. This review aims to cover a few topics in liver lesions, FNAC Vs core biopsy, IHC, Margin examination, and frozen sections, in order to improve the communication between these two specialities.


Neuropathology | 2017

Spindle cell oncocytoma of adenohypophysis: Review of literature and report of another recurrent case

Akash Sali; Sridhar Epari; Chandralekha Tampi; Atul Goel

Spindle cell oncocytoma (SCO) of adenohypophysis was first described in 2002 by Roncaroli et al. as a new entity in the tumors originating from adenohypophysis. It was subsequently recognized as a distinct entity in the 2007 WHO classification of CNS tumors and retained in the current updated classification. In contrast to that suggested by the original authors, this tumor does have a potential for recurrence as first described by Kloub et al. and later with many such case reports. This tumor can be confused with other sellar tumors like pituicytomas and pituitary adenoma, both radiologically and histopathologically. However, it is imperative to differentiate these tumors from the above‐mentioned differential diagnoses as it certainly has a recurrent potential. To date only 34 cases of SCO have been published in the English literature. Herein we present a rare SCO case with unusually aggressive course in a 64‐year‐old man, which recurred 4 years after the initial diagnosis.


ABCD. Arquivos Brasileiros de Cirurgia Digestiva (São Paulo) | 2017

BRUNNER GLAND ADENOMA MASQUERADING AS DUODENAL GASTROINTESTINAL STROMAL TUMOR WITH INTUSSUSCEPTION: CASE REPORT

Gunjan Desai; Kamal Sunder Yadav; Prasad Pande; Priyanka Akhilesh Sali; Chandralekha Tampi; Prasad Wagle

Brunner gland adenoma (Brunerroma or hamartoma) is a rare, benign lesion of the Brunner’s glands, accounting for 10.6% of benign duodenal tumors10. It is predominantly seen in the 5th to 6th decades and with no gender predilection13. It is often an incidental finding during esophagogastroduodenoscopy or imaging studies. In symptomatic patients, clinical manifestations include gastrointestinal bleeding, duodenal obstruction, abdominal pain, ampullary obstruction, or intussusception8,9. Given their potential to be mistaken as cancer, it is important to consider it in the differential diagnosis of duodenal masses14. As there have been reports of focal cellular atypia and adenocarcinoma within the lesion, resection, whether endoscopic or surgical is recommended for suspected Brunneromas3. We report here a case of Brunneroma, which presented as gastrointestinal stromal tumor (GIST) with intussusception on radiological and endoscopic studies and brief review of literature.


Indian Journal of Medical and Paediatric Oncology | 2009

Squamous cell carcinoma of tongue in a renal transplant recipient.

Pavan Malleshappa; Manjurhusen Aghariya; Chandralekha Tampi; Bharat V. Shah

The overall incidence of malignancies in post renal transplant recipients is reported to be approximately 5 to 6%. Malignancies are significant complications after transplantation. Common malignancies include malignancies of the skin and post-transplant lymphoproliferative disorder (PTLD). Squamous cell carcinoma of the tongue is very rare. We present a case of squamous cell carcinoma of the tongue developing nine years after renal transplantation, in a 30-year-old man. He underwent left hemiglossectomy initially and then modified neck dissection. His graft function continues to remain stable.

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Palepu Jagannath

Lilavati Hospital and Research Centre

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Prashant Mullerpatan

Lilavati Hospital and Research Centre

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R. Shah

Lilavati Hospital and Research Centre

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Kamal Sunder Yadav

Lilavati Hospital and Research Centre

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Priyanka Akhilesh Sali

Lilavati Hospital and Research Centre

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Vatsala M. Doctor

Lilavati Hospital and Research Centre

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