Abdul Abid

ORCID: 0009-0003-0417-1843
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About
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Research Areas
  • Renal Diseases and Glomerulopathies
  • Lipoproteins and Cardiovascular Health
  • Chronic Kidney Disease and Diabetes
  • Nonmelanoma Skin Cancer Studies
  • Sarcoma Diagnosis and Treatment
  • Hematological disorders and diagnostics
  • Cardiac Arrhythmias and Treatments
  • Genetic factors in colorectal cancer
  • Cutaneous lymphoproliferative disorders research
  • Colorectal Cancer Treatments and Studies
  • Cancer Genomics and Diagnostics
  • Coronary Artery Anomalies
  • Kawasaki Disease and Coronary Complications
  • Occupational and environmental lung diseases
  • Folklore, Mythology, and Literature Studies
  • Atrial Fibrillation Management and Outcomes
  • Intraperitoneal and Appendiceal Malignancies
  • Culinary Culture and Tourism
  • Myasthenia Gravis and Thymoma
  • Lung Cancer Treatments and Mutations
  • Venous Thromboembolism Diagnosis and Management
  • Neurofibromatosis and Schwannoma Cases
  • Interstitial Lung Diseases and Idiopathic Pulmonary Fibrosis
  • Sexual Differentiation and Disorders
  • Acute Myocardial Infarction Research

University of Virginia
2023-2024

The University of Texas Medical Branch at Galveston
2019-2022

University of Bologna
2022

Cleveland Clinic
2022

Memorial Sloan Kettering Cancer Center
2022

Massachusetts General Hospital
2022

Newark Academy
2021

University of Minnesota Rochester
2021

Texas Oncology
2021

Philadelphia University
2021

Abstract Background Muir–Torre syndrome (MTS) is a rare genetic disorder that caused by mismatch repair (MMR) protein mutations. MTS increases the risk of developing skin and gastrointestinal tumors such as sebaceous adenomas (SAs), carcinomas, colorectal cancer, endometrial ovarian cancer. The these types varies depending on involved mutation individual's family history risk. Case Presentation A 47‐year‐old male presented with multiple lesions scalp, face, flank, back. examination revealed...

10.1002/jso.27440 article EN cc-by-nc Journal of Surgical Oncology 2023-09-14

Lipoprotein glomerulopathy is an infrequent glomerular disorder that culminates in nephrotic syndrome and often progresses to kidney failure. Whereas most patients have been reported Japan China, limited reports documented outside these regions. This patient represents the first report of lipoprotein Pakistan.

10.1177/10668969241228298 article EN International Journal of Surgical Pathology 2024-02-07

Abstract Background Myxoid neurofibromas (NF) are uncommon, benign spindle cell tumors that originate from peripheral nerve sheaths, often posing a diagnostic challenge due to their hypocellularity on cytology specimens. Distinguishing myxoid lesions can be challenging, given the broad range of potential differential diagnoses. Case Presentation A 26‐year‐old female with past medical history embolized inguinal, flank, and retroperitoneal venolymphatic malformation presented left pelvic pain...

10.1002/dc.25288 article EN cc-by-nc Diagnostic Cytopathology 2024-02-16

Malignant pleural mesothelioma (MPM) is a rare but aggressive malignancy with poor prognosis. Because of this tumor rarity and overlapping histologic features other types, the histopathological findings diagnostic immunohistochemical workup are essential in establishing final diagnosis MPMs. We aimed to review criteria, WHO classification updates, staining markers value achieve an appropriate clinical diagnosis.

10.1002/dc.25053 article EN Diagnostic Cytopathology 2022-09-07

Background: Coronary artery ectasia (CAE) is frequently observed in patients undergoing coronary angiogrphy for evaluation of disease (CAD).It not clear whether CAE a variant CAD or separate entity.Objective: To compare the clinical and angiographic profile having with those stenotic (CAD). Materials And Methods:We studied 1176 consecutive who had angiography various indications.Of these 297 were excluded because incomplete data.The remaining 879 divided into two groups Artery Ectasia Group...

10.15406/jccr.2017.09.00328 article EN cc-by-nc Journal of Cardiology & Current Research 2017-07-25

Bronchogenic cysts are rare, congenital malformations of the foregut, most commonly located in mediastinum. Subcutaneous bronchogenic exceedingly rare. We report an 11-month-old boy who presented with asymptomatic chest wall mass. He underwent surgical excision and final histopathology was consistent a cyst. To our knowledge, this is first reported case subcutaneous cyst child.

10.1016/j.epsc.2019.101337 article EN cc-by-nc-nd Journal of Pediatric Surgery Case Reports 2019-11-06

Balloon cell melanoma (BCM) is an exceptionally uncommon histological variant, making up <1% of all malignant melanomas. Diagnosing balloon on cytological specimens can be challenging due to its scarcity and similarity other medical conditions. A comprehensive clinical assessment analysis, coupled with immunohistochemical staining, play a crucial role in distinguishing from various benign skin The differential diagnoses encompass spitz nevus, clear sarcoma tendons aponeuroses (melanoma...

10.1111/cyt.13354 article EN cc-by-nc Cytopathology 2024-01-09

Eccrine spiradenoma (ES) is an uncommon and benign adnexal tumour originating from sweat glands. The cytological examination of ES poses a diagnostic challenge, as it can be mistaken for various malignant basaloid skin neoplasms. cytomorphologic features are infrequently documented in existing literature. This study seeks to present thorough exploration the traits associated with ES, accompanied by analysis ancillary testing that contribute accurate identification this entity specimens....

10.1111/cyt.13348 article EN cc-by Cytopathology 2023-12-12

Testicular adrenal rest tumors are a rare development of patients with congenital hyperplasia. It is difficult to diagnose due similarities Leydig cell tumors. Treatment can be conservative or surgical. We describe the case 56 year old male presenting bilateral testicular pain and irregular growth that was managed unilateral orchiectomy. analyzed distinguishing factors compared tumors, as well diagnostic treatment methods.

10.1016/j.eucr.2022.102247 article EN cc-by-nc-nd Urology Case Reports 2022-09-26

Pulmonary adenocarcinoma is the most prevalent carcinoma of lung and constitutes five main histologic patterns including acinar, papillary, micropapillary, lepidic, solid growth pattern. Mucinous non-mucinous subtypes are routinely seen. The presence abundant associated psammoma bodies a rare feature seen in approximately 7.2% pulmonary cases. Abundant commonly observed various tumors such as papillary carcinomas thyroid gland,1 ovarian serous adenocarcinomas,2 mesothelioma rarely other...

10.1002/dc.25208 article EN cc-by-nc Diagnostic Cytopathology 2023-08-03

Presacral myelolipoma is an uncommon benign tumor, and its diagnosis can be challenging oncytology specimens. This case emphasizes the importance of fine needle aspiration cytology as initial valuable diagnostic tool for evaluating presacral masses. The identification a combination mature adipose tissue hematopoietic elements in varying proportions crucial feature FNA cytology. underscores role providing accurate guiding subsequent management decisions.

10.1111/cyt.13341 article EN cc-by Cytopathology 2023-12-04
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