Fahir Özkalemkaş

Dr. Fahir Özkalemkaş

orcid

Research Focus & Metrics

Academic Career Length

27Years (2000-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 November 2005 in BMC Cancer
Verified
Journal Article
Open access
PDF file
FÖFahir Özkalemkaş
Fahir Özkalemkaş
RARıdvan Ali
Rıdvan Ali
VOVildan Ozkocaman
Vildan Ozkocaman
TOTulay Ozcelik
Tulay Ozcelik
UOUlku Ozan
Ulku Ozan
ATAhmet Tunali
Ahmet Tunali
Background: Although bone marrow metastases can be found commonly in some malignant tumors, diagnosing a nonhematologic malignancy from marrow is not a usual event. Methods: To underscore the value of bone marrow aspiration and biopsy as a short cut in establishing a diagnosis for disseminated tumors, we reviewed 19 patients with nonhematologic malignancies who initially had diagnosis from bone marrow. Results: The main indications for bone marrow examination were microangiopathic hemolytic anemia (MAHA), leukoerythroblastosis (LEB) and unexplained cytopenias. Bone marrow aspiration was not diagnostic due to dry tap or inadequate material in 6 cases. Biopsy results were parallel to the cytological ones in all cases except one; however a meticulous second examination of the biopsy confirmed the cytologic diagnosis in this patient too. The most common histologic subtype was adenocarcinoma, and after all the clinical and laboratory evaluations, the primary focus was disclosed definitively in ten patients (5 stomach, 3 prostate, 1 lung, 1 muscle) and probably in four patients (3 gastrointestinal tract, 1 lung). All work up failed in five patients and these cases were classified as tumor of unknown origin (TUO). Conclusion: Our series showed that anemia, thrombocytopenia, elevated red cell distribution width (RDW) and hypoproteinemia formed a uniform tetrad in patients with disseminated tumors that were diagnosed via bone marrow examination. The prognosis of patients was very poor and survivals were only a few days or weeks (except for 4 patients whose survivals were longer). We concluded that MAHA, LEB and unexplained cytopenias are strong indicators of the necessity of bone marrow examination. Because of the very short survival of many patients, all investigational procedures should be judged in view of their rationality, and should be focused on treatable primary tumors.

1 December 2020 in Leukemia Research
Verified
Journal Article
Closed access
TKTugcan Alp Kirkizlar
Tugcan Alp Kirkizlar
EAEMİN HALİS Akalin
EMİN HALİS Akalin
HKHakki Onur Kirkizlar
Hakki Onur Kirkizlar
FÖFahir Özkalemkaş
Fahir Özkalemkaş
VOVildan Ozkocaman
Vildan Ozkocaman
RARıdvan Ali
Rıdvan Ali

6 September 2004 in Annals of Clinical Microbiology and Antimicrobials
Verified
Journal Article
Open access
PDF file
FÖFahir Özkalemkaş
Fahir Özkalemkaş
RARidvan Ali
Ridvan Ali
AOAtilla Ozkan
Atilla Ozkan
TOTulay Ozcelik
Tulay Ozcelik
VOVildan Ozkocaman
Vildan Ozkocaman
HAHalis Akalin
Halis Akalin
Background: Although various hematologic abnormalities are seen in tuberculosis, immune thrombocytopenic purpura is a rare event. Case Presentation: We report a case of a 29 year-old male who was presented with immune thrombocytopenia-induced hemoptysis, macroscopic hematuria and generalized petechiae. The patient was found to have clinical, microbiological and radiological evidence of active pulmonary tuberculosis. The immune thrombocytopenic purpura was successfully treated with anti-tuberculous drugs combined with corticosteroids and high dose immune globulin therapy. Conclusion: Immune thrombocytopenic purpura can be one of the hematological manifestations of tuberculosis which has a global prevalence with increasing incidence secondary to HIV infection.

1 January 2022 in Mediterranean Journal of Hematology and Infectious Diseases
Verified
Journal Article
Open access
PDF file
BOBedrettin Orhan
Bedrettin Orhan
FÖFahir Özkalemkaş
Fahir Özkalemkaş
VÖVildan Özkocaman
Vildan Özkocaman
BGBüşra Gürbüz
Büşra Gürbüz
TETUBA ERSAL
TUBA ERSAL
RARıdvan Ali
Rıdvan Ali
Background and Objective: Perianal pathologies are the most common cause of perianal infections in patients with hematological malignancies. Perianal infection diagnosis in this group of patients is difficult, thus careful anorectal examination is necessary, with imaging modalities. The literature revealed a knowledge gap on the approach of anal pathologies in patients with neutropenia during diagnosis or chemotherapy. This study aimed to examine our institutional data of perianal complications and investigate the relationship among the white blood cell-neutrophil count, perianal lesion, and the type of treatment in patients with hematologic malignancies during the neutropenic period. Methods: Patients with a hematologic malignancy, hospitalized for cytotoxic chemotherapy, complicated by perianal pathology, and documented by at least one imaging method were included in the study. Results: A total of 42 patients were included in the study. The comparison between the groups revealed no statistical significance between the anal abscess formation and the neutrophil count and previous perianal pathology. A statistical significance in favor of acute myeloid leukemia was found between patient diagnosis and anal abscess development. An inverse relationship was found between the number of white blood cells at hospitalization and having an anal pathology operation. It was observed that patients with high white blood cell count were less operated on due to anal pathology. Conclusions: In conclusion, this article has shown that white blood cell count at the time of hospitalization in patients with hematological malignancy, can affect the operation status of patients due to anal pathologies that may occur in the neutropenic period.

1 January 2006 in Annals of Clinical Microbiology and Antimicrobials
Verified
Journal Article
Open access
RARidvan Ali
Ridvan Ali
FÖFahir Özkalemkaş
Fahir Özkalemkaş
TOTulay Ozcelik
Tulay Ozcelik
VOVildan Ozkocaman
Vildan Ozkocaman
AOAtilla Ozkan
Atilla Ozkan
ATAhmet Tunali
Ahmet Tunali
Aspergillus is a ubiquitous soil-dwelling fungus known to cause significant pulmonary infection in immunocompromised patients. The incidence of aspergillosis has increased during the past two decades and is a frequently lethal complication of acute leukemia patients that occurs following both chemotherapy and bone marrow transplantation. The diagnosis of invasive pulmonary aspergillosis (IPA) according to the criteria that are established by European Organization for the Research and Treatment of Cancer and Mycoses Study Group raise difficulties in severely ill patients. Despite established improvements in field of diagnosis (galactomannan antigen, quantitative PCR, real-time PCR for Aspergillus spp., and findings of computed tomography) and treatment with new antifungals, it is still a major problem in patients with acute leukemia. However, prompt and effective treatment of IPA is crucial because most patients will need subsequent chemotherapy for underlying hematologic disease as soon as possible. We report a 33-year-old male patient with acute promyelocytic leukemia diagnosed in 1993 that developed invasive pulmonary aspergillosis due to A. flavus at relapse in 2003. The patient was successfully treated with liposomal amphotericin B and underwent surgical pulmonary resection. The operative course was uneventful. This report emphasizes the clinical picture, applicability of recent advances in diagnostic and therapeutic approaches for IPA. For early identification of a patient infected with IPA, a high index of suspicion and careful clinical and radiological examinations with serial screening for galactomannan should be established. If aspergillosis is suspected, anti-aspergillosis drug should be administered immediately, and if a unique pulmonary lesion remains, surgical resection should be considered to prevent reactivation during consecutive chemotherapy courses and to improve the outcome.

10 August 2006 in Journal of Clinical Oncology
Verified
Journal Article
Open access
RARidvan Ali
Ridvan Ali
FÖFahir Özkalemkaş
Fahir Özkalemkaş
TOTulay Ozcelik
Tulay Ozcelik
VOVildan Ozkocaman
Vildan Ozkocaman
AOAtilla Ozkan
Atilla Ozkan