scholarly journals Mixed connective tissue disorder in a patient with retroviral disease: A rare case report

2021 ◽  
Vol 5 (1) ◽  
pp. 95
Author(s):  
FarhanaTahseen Taj ◽  
Monika Singh
Keyword(s):  
Case Report ◽  
Connective Tissue ◽  
Rare Case ◽  
Connective Tissue Disorder ◽  
Rare Case Report ◽  
Mixed Connective Tissue Disorder

scholarly journals Distal Renal Tubular Acidosis as complication of Mixed Connective Tissue Disorder with autoimmune hypothyroidism- a case report

2016 ◽  
Vol 27 (1) ◽  
pp. 37-39
Author(s):  
Md Daharul Islam ◽  
SM Tajdit Rahman ◽  
Khaleda Akter ◽  
Md Azizul Hoque
Keyword(s):  
Case Report ◽  
Connective Tissue ◽  
Renal Tubular Acidosis ◽  
Connective Tissue Disorder ◽  
Distal Renal Tubular Acidosis ◽  
Undifferentiated Connective Tissue Disease ◽  
Acid Transport ◽  
Autoimmune Hypothyroidism ◽  
Renal Tubular ◽  
Mixed Connective Tissue Disorder

Renal tubular acidosis (RTA) is a constellation of syndromes arising from different derangements of tubular acid transport. Multiple associations have been established with renal tubular acidosis. We report a case of distal renal tubular acidosis which may be associated with undifferentiated connective tissue disease in which patient is also having autoimmune hypothyroidism along with that is not very common.Bangladesh J Medicine Jan 2016; 27(1) : 37-39

scholarly journals Autoamputation and Polyneuropathy in Mixed Connective Tissue Disorder: A Case Report

Cureus ◽  
2017 ◽  
Author(s):  
Syeda Naqvi ◽  
Vikash Talib ◽  
Razia Aijaz ◽  
Zeeshan Ali ◽  
Shehroz Bashir ◽  
...  
Keyword(s):  
Case Report ◽  
Connective Tissue ◽  
Connective Tissue Disorder ◽  
Mixed Connective Tissue Disorder

Cervical chondroma in a 1.8-year-old child - rare case report

ORL ro ◽  
2016 ◽  
Vol 2 (1) ◽  
pp. 10-11
Author(s):  
Adina A. Zamfir-Chiru-Anton ◽  
D.C. Gheorghe
Keyword(s):  
Case Report ◽  
Connective Tissue ◽  
Rare Case ◽  
Typical Case ◽  
Long Bones ◽  
Rare Case Report

Chondroma is a benign encapsulated tumor, firm at palpation and multilobulated. Histologically it develops from connective tissue. It is composed of chondrocytes producing an amorphous basophilic matrix. It tends to replace surrounding tissues, with medium severity local aggression. Neck chondromas are extremely rare, their origin being in a typical case the long bones periosteum (over 60% of cases). The authors present a rare case of anterior cervical chondroma, in a 1.8-year-old child. 

scholarly journals A rare case of Ehler Danlos syndrome - Progeroid type: a case report

2016 ◽  
Vol 4 (1) ◽  
pp. 261
Author(s):  
G. Fatima Shirly Anitha ◽  
V. Karthik Shanmugam ◽  
V. Vignesh Rajendran
Keyword(s):  
Case Report ◽  
Connective Tissue ◽  
Old Age ◽  
Clinical Features ◽  
Rare Diseases ◽  
Rare Case ◽  
Type A ◽  
Connective Tissue Disorder ◽  
Rare Type ◽  
Danlos Syndrome

Ehler Danlos syndrome (EDS), is a group of genetically heterogenous connective tissue disorder. A very rare type of this syndrome is the Progeroid type which is included in the NIH group of rare diseases list. The prevalence is < 1 / 1000000. Along with the usual clinical features, patients with Ehler Danlos syndrome-Progeroid type have old age appearance. Here we report one such rare case of this syndrome diagnosed in a 8 yr old child with characteristic clinical features and supportive genetic confirmation.  

scholarly journals Castleman’s disease associated with mixed connective tissue disorder and cerebral ischaemia and vasculitis: A rare case and a diagnostic challenge for an infectologist

2020 ◽  
Vol 77 (8) ◽  
pp. 872-877
Author(s):  
Lidija Popovic-Dragonjic ◽  
Maja Jovanovic ◽  
Miodrag Vrbic ◽  
Maja Stanojevic ◽  
Miljan Krstic ◽  
...  
Keyword(s):  
Case Report ◽  
Lymph Node ◽  
Connective Tissue ◽  
Castleman’S Disease ◽  
Connective Tissue Disorder ◽  
Castleman's Disease ◽  
Diagnostic Challenge ◽  
Systemic Involvement ◽  
Similar Appearance ◽  
Mixed Connective Tissue Disorder

Introduction. Castleman's disease (CD) or angiofolicullar lymph node hyperplasia is a rare pathologic process characterized by non-neoplastic reactive proliferation of lymphoid tissue. Mimicking clinical and laboratory signs of infection, it could be a great diagnostic problem for an infectologist. Case report. We report a case of a 39-year old man who was initially clinically suspected to have an infectious central nervous system (CNS) affection, having most similar appearance to neurotuberculosis. Malignancy with bone metastases and lymphoma were also among many possible diagnoses. The patient was later histologically confirmed to have Castleman's disease, analyzing the enlarged inguinal lymph node, which was the key point in rejecting the suspicion of malignancy and tuberculosis. By further analyses, the patient was diagnosed to have mixed connective tissue disorder (MCTD). Vasculitis of mesencephalon and thalamus was detected by magnetic resonance imaging. Conclusion. CD with CNS involvement is very rare as well as CD with MCTD association, making this case even more unique. This case report underlines the importance of definitive histological diagnosis in patients with lymphadenopathia associated with systemic involvement and the need of additional immunological and radiological examinations, as well.

scholarly journals Focal fibrous hyperplasia beneath the tongue – A rare case report

2021 ◽  
Vol 6 (3) ◽  
pp. 124-127
Author(s):  
Mohammed Ahsan Razi ◽  
Surangama Debnath ◽  
Bimal Chandra Kirtaniya ◽  
Seema Qamar
Keyword(s):  
Case Report ◽  
Connective Tissue ◽  
Oral Cavity ◽  
Male Patient ◽  
Rare Case ◽  
Ventral Surface ◽  
Present Case Report ◽  
Tissue Tumor ◽  
Rare Case Report ◽  
Slow Growing

Focal fibrous hyperplasia is a slow growing connective tissue tumor that frequently occurs in different anatomic sites of the oral cavity. The present case report describes the occurrence of this lesion on the ventral surface of the tongue which is hitherto least reported intraoral site, in a 11 year old male patient, which was successfully excised.

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